Canonical Allele Identifier: CA2499217081

Gene: MFSD8

Linked Data

• ClinVar Variation Id: 1074190
• ClinVar RCV Id: RCV001387412
• dbSNP Id: rs2148839459
• gnomAD v4: 4-127921551-ATATAGAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.127921557_127921563del , CM000666.2:g.127921557_127921563del	GRCh38
NC_000004.11:g.128842712_128842718del , CM000666.1:g.128842712_128842718del	GRCh37
NC_000004.10:g.129062162_129062168del	NCBI36
NG_008657.1:g.49427_49433del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296468.8:c.1316_1322del	ENSP00000296468.3:p.Thr439IlefsTer5
ENST00000509826.2:c.*637_*643del	ENSP00000421176.2:n.*637_*643del
ENST00000513559.6:c.1034_1040del	ENSP00000425000.2:p.Thr345IlefsTer5
ENST00000515130.6:c.*201_*207del	ENSP00000493056.1:n.*201_*207del
ENST00000641025.1:c.*201_*207del	ENSP00000493346.1:n.*201_*207del
ENST00000641092.1:c.*201_*207del	ENSP00000493392.1:n.*201_*207del
ENST00000641133.1:c.*630_*636del	ENSP00000493192.1:n.*630_*636del
ENST00000641146.1:n.1182_1188del
ENST00000641147.1:c.866_872del	ENSP00000493133.1:p.Thr289IlefsTer5
ENST00000641178.1:c.1181_1187del	ENSP00000492989.1:p.Thr394IlefsTer5
ENST00000641186.1:c.1202_1208del	ENSP00000493347.1:p.Thr401IlefsTer5
ENST00000641228.1:c.*201_*207del	ENSP00000493194.1:n.*201_*207del
ENST00000641332.1:c.*377_*383del	ENSP00000493397.1:n.*377_*383del
ENST00000641340.1:c.*445_*451del	ENSP00000493191.1:n.*445_*451del
ENST00000641388.1:n.563_569del
ENST00000641393.1:c.866_872del	ENSP00000493197.1:p.Thr289IlefsTer5
ENST00000641397.1:c.*201_*207del	ENSP00000493406.1:n.*201_*207del
ENST00000641413.1:c.241_247del
ENST00000641434.1:c.1316_1322del	ENSP00000493279.1:p.Thr439IlefsTer5
ENST00000641464.1:c.*549_*555del	ENSP00000493438.1:n.*549_*555del
ENST00000641482.1:c.*201_*207del	ENSP00000493277.1:n.*201_*207del
ENST00000641508.1:c.*549_*555del	ENSP00000493209.1:n.*549_*555del
ENST00000641509.1:c.1001_1007del	ENSP00000493459.1:p.Thr334IlefsTer5
ENST00000641590.1:c.*201_*207del	ENSP00000493132.1:n.*201_*207del
ENST00000641658.1:c.*481_*487del	ENSP00000492987.1:n.*481_*487del
ENST00000641686.2:c.1316_1322del MANE Select	ENSP00000493218.2:p.Thr439IlefsTer5
ENST00000641690.1:c.1115_1121del	ENSP00000492966.1:p.Thr372IlefsTer5
ENST00000641742.1:c.*481_*487del	ENSP00000493315.1:n.*481_*487del
ENST00000641748.1:c.1316_1322del	ENSP00000493330.1:p.Thr439IlefsTer5
ENST00000641753.1:c.1143_1149del
ENST00000641774.1:c.*568_*574del	ENSP00000492960.1:n.*568_*574del
ENST00000641830.1:c.548_554del
ENST00000641843.1:c.*377_*383del	ENSP00000493174.1:n.*377_*383del
ENST00000641869.1:c.517_523del
ENST00000641870.1:c.*377_*383del	ENSP00000493044.1:n.*377_*383del
ENST00000641882.1:c.*481_*487del	ENSP00000493301.1:n.*481_*487del
ENST00000641928.1:c.*445_*451del	ENSP00000493418.1:n.*445_*451del
ENST00000641949.1:c.554-722_554-716del	ENSP00000492891.1:n.554-722_554-716del
ENST00000642012.1:n.1180_1186del
ENST00000642034.1:c.*201_*207del	ENSP00000493285.1:n.*201_*207del
ENST00000642042.1:c.1316_1322del	ENSP00000493260.1:p.Thr439IlefsTer5
ENST00000642078.1:c.*377_*383del	ENSP00000492885.1:n.*377_*383del
ENST00000296468.7:c.1316_1322del	ENSP00000296468.3:p.Thr439IlefsTer5
ENST00000504126.1:n.344_350del
ENST00000513559.5:c.1181_1187del	ENSP00000425000.1:p.Thr394IlefsTer5
ENST00000515130.5:n.1658_1664del
NM_152778.2:c.1316_1322del	NP_689991.1:p.Thr439IlefsTer5
XM_005262893.1:c.1316_1322del	XP_005262950.1:p.Thr439IlefsTer5
XM_005262896.1:c.1169_1175del	XP_005262953.1:p.Thr390IlefsTer5
XM_005262897.1:c.1115_1121del	XP_005262954.1:p.Thr372IlefsTer5
XM_005262898.2:c.*201_*207del	XP_005262955.1:n.*201_*207del
XM_011531830.1:c.1202_1208del	XP_011530132.1:p.Thr401IlefsTer5
XM_011531831.1:c.1001_1007del	XP_011530133.1:p.Thr334IlefsTer5
XM_011531832.1:c.*201_*207del	XP_011530134.1:n.*201_*207del
XR_938717.1:n.1393_1399del
NM_001363520.1:c.1115_1121del	NP_001350449.1:p.Thr372IlefsTer5
NM_001363521.1:c.1001_1007del	NP_001350450.1:p.Thr334IlefsTer5
XM_005262898.3:c.*201_*207del	XP_005262955.1:n.*201_*207del
XM_017007989.1:c.*201_*207del	XP_016863478.1:n.*201_*207del
XM_024453981.1:c.1181_1187del	XP_024309749.1:p.Thr394IlefsTer5
XM_024453982.1:c.1067_1073del	XP_024309750.1:p.Thr356IlefsTer5
XM_024453983.1:c.866_872del	XP_024309751.1:p.Thr289IlefsTer5
XR_001741194.1:n.1289_1295del
XR_001741195.1:n.1175_1181del
XR_001741196.1:n.1088_1094del
XR_001741197.1:n.1248_1254del
XR_001741198.2:n.1144_1150del
XR_001741199.1:n.1144_1150del
XR_938717.2:n.1393_1399del
NM_001363520.2:c.1115_1121del	NP_001350449.1:p.Thr372IlefsTer5
NM_001363521.2:c.1001_1007del	NP_001350450.1:p.Thr334IlefsTer5
NM_001371590.1:c.1181_1187del	NP_001358519.1:p.Thr394IlefsTer5
NM_001371591.1:c.1316_1322del	NP_001358520.1:p.Thr439IlefsTer5
NM_001371592.1:c.1322_1328del	NP_001358521.1:p.Thr441IlefsTer5
NM_001371593.1:c.1202_1208del	NP_001358522.1:p.Thr401IlefsTer5
NM_001371594.1:c.1169_1175del	NP_001358523.1:p.Thr390IlefsTer5
NM_001371595.1:c.1034_1040del	NP_001358524.1:p.Thr345IlefsTer5
NM_001371596.2:c.1316_1322del MANE Select	NP_001358525.1:p.Thr439IlefsTer5
NM_152778.3:c.1316_1322del	NP_689991.1:p.Thr439IlefsTer5
NM_152778.4:c.1316_1322del	NP_689991.1:p.Thr439IlefsTer5