Canonical Allele Identifier: CA358171543

Gene: MFSD8

Linked Data

• gnomAD v4: 4-127921770-A-C
• MyVariant Identifiers: chr4:g.128842925A>C (hg19) ; chr4:g.127921770A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.127921770A>C , CM000666.2:g.127921770A>C	GRCh38
NC_000004.11:g.128842925A>C , CM000666.1:g.128842925A>C	GRCh37
NC_000004.10:g.129062375A>C	NCBI36
NG_008657.1:g.49215T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296468.8:c.1104T>G	ENSP00000296468.3:p.Asp368Glu
ENST00000509826.2:c.*425T>G	ENSP00000421176.2:n.*425T>G
ENST00000513559.6:c.822T>G	ENSP00000425000.2:p.Asp274Glu
ENST00000515130.6:c.865T>G	ENSP00000493056.1:p.Phe289Val
ENST00000641025.1:c.1000T>G	ENSP00000493346.1:p.Phe334Val
ENST00000641092.1:c.799T>G	ENSP00000493392.1:p.Phe267Val
ENST00000641133.1:c.*418T>G	ENSP00000493192.1:n.*418T>G
ENST00000641146.1:n.970T>G
ENST00000641147.1:c.654T>G	ENSP00000493133.1:p.Asp218Glu
ENST00000641178.1:c.969T>G	ENSP00000492989.1:p.Asp323Glu
ENST00000641186.1:c.990T>G	ENSP00000493347.1:p.Asp330Glu
ENST00000641228.1:c.799T>G	ENSP00000493194.1:p.Phe267Val
ENST00000641332.1:c.*165T>G	ENSP00000493397.1:n.*165T>G
ENST00000641340.1:c.*233T>G	ENSP00000493191.1:n.*233T>G
ENST00000641388.1:n.351T>G
ENST00000641393.1:c.654T>G	ENSP00000493197.1:p.Asp218Glu
ENST00000641397.1:c.685T>G	ENSP00000493406.1:p.Phe229Val
ENST00000641413.1:c.29T>G
ENST00000641434.1:c.1104T>G	ENSP00000493279.1:p.Asp368Glu
ENST00000641464.1:c.*337T>G	ENSP00000493438.1:n.*337T>G
ENST00000641482.1:c.1000T>G	ENSP00000493277.1:p.Phe334Val
ENST00000641508.1:c.*337T>G	ENSP00000493209.1:n.*337T>G
ENST00000641509.1:c.789T>G	ENSP00000493459.1:p.Asp263Glu
ENST00000641590.1:c.886T>G	ENSP00000493132.1:p.Phe296Val
ENST00000641658.1:c.*269T>G	ENSP00000492987.1:n.*269T>G
ENST00000641686.2:c.1104T>G MANE Select	ENSP00000493218.2:p.Asp368Glu
ENST00000641690.1:c.903T>G	ENSP00000492966.1:p.Asp301Glu
ENST00000641742.1:c.*269T>G	ENSP00000493315.1:n.*269T>G
ENST00000641748.1:c.1104T>G	ENSP00000493330.1:p.Asp368Glu
ENST00000641753.1:c.931T>G
ENST00000641774.1:c.*356T>G	ENSP00000492960.1:n.*356T>G
ENST00000641830.1:c.336T>G
ENST00000641843.1:c.*165T>G	ENSP00000493174.1:n.*165T>G
ENST00000641869.1:c.305T>G
ENST00000641870.1:c.*165T>G	ENSP00000493044.1:n.*165T>G
ENST00000641882.1:c.*269T>G	ENSP00000493301.1:n.*269T>G
ENST00000641928.1:c.*233T>G	ENSP00000493418.1:n.*233T>G
ENST00000641949.1:c.554-934T>G	ENSP00000492891.1:n.554-934T>G
ENST00000642012.1:n.968T>G
ENST00000642034.1:c.886T>G	ENSP00000493285.1:p.Phe296Val
ENST00000642042.1:c.1104T>G	ENSP00000493260.1:p.Asp368Glu
ENST00000642078.1:c.*165T>G	ENSP00000492885.1:n.*165T>G
ENST00000296468.7:c.1104T>G	ENSP00000296468.3:p.Asp368Glu
ENST00000504126.1:n.132T>G
ENST00000505284.5:n.895T>G
ENST00000513559.5:c.969T>G	ENSP00000425000.1:p.Asp323Glu
ENST00000515130.5:n.1446T>G
NM_152778.2:c.1104T>G	NP_689991.1:p.Asp368Glu
XM_005262893.1:c.1104T>G	XP_005262950.1:p.Asp368Glu
XM_005262896.1:c.957T>G	XP_005262953.1:p.Asp319Glu
XM_005262897.1:c.903T>G	XP_005262954.1:p.Asp301Glu
XM_005262898.2:c.1000T>G	XP_005262955.1:p.Phe334Val
XM_011531830.1:c.990T>G	XP_011530132.1:p.Asp330Glu
XM_011531831.1:c.789T>G	XP_011530133.1:p.Asp263Glu
XM_011531832.1:c.886T>G	XP_011530134.1:p.Phe296Val
XR_938717.1:n.1181T>G
NM_001363520.1:c.903T>G	NP_001350449.1:p.Asp301Glu
NM_001363521.1:c.789T>G	NP_001350450.1:p.Asp263Glu
XM_005262898.3:c.1000T>G	XP_005262955.1:p.Phe334Val
XM_017007989.1:c.799T>G	XP_016863478.1:p.Phe267Val
XM_024453981.1:c.969T>G	XP_024309749.1:p.Asp323Glu
XM_024453982.1:c.855T>G	XP_024309750.1:p.Asp285Glu
XM_024453983.1:c.654T>G	XP_024309751.1:p.Asp218Glu
XR_001741194.1:n.1077T>G
XR_001741195.1:n.963T>G
XR_001741196.1:n.876T>G
XR_001741197.1:n.1036T>G
XR_001741198.2:n.932T>G
XR_001741199.1:n.932T>G
XR_938717.2:n.1181T>G
NM_001363520.2:c.903T>G	NP_001350449.1:p.Asp301Glu
NM_001363521.2:c.789T>G	NP_001350450.1:p.Asp263Glu
NM_001371590.1:c.969T>G	NP_001358519.1:p.Asp323Glu
NM_001371591.1:c.1104T>G	NP_001358520.1:p.Asp368Glu
NM_001371592.1:c.1110T>G	NP_001358521.1:p.Asp370Glu
NM_001371593.1:c.990T>G	NP_001358522.1:p.Asp330Glu
NM_001371594.1:c.957T>G	NP_001358523.1:p.Asp319Glu
NM_001371595.1:c.822T>G	NP_001358524.1:p.Asp274Glu
NM_001371596.2:c.1104T>G MANE Select	NP_001358525.1:p.Asp368Glu
NM_152778.3:c.1104T>G	NP_689991.1:p.Asp368Glu
NM_152778.4:c.1104T>G	NP_689991.1:p.Asp368Glu