Canonical Allele Identifier: CA2573138005
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1456161
ClinVar RCV Id: RCV001951006
dbSNP Id: rs2148839909

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.127921645dup , CM000666.2:g.127921645dup GRCh38
NC_000004.11:g.128842800dup , CM000666.1:g.128842800dup GRCh37
NC_000004.10:g.129062250dup NCBI36
NG_008657.1:g.49340dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000296468.8:c.1229dup ENSP00000296468.3:p.Tyr410Ter
ENST00000509826.2:c.*550dup ENSP00000421176.2:n.*550dup
ENST00000513559.6:c.947dup ENSP00000425000.2:p.Tyr316Ter
ENST00000515130.6:c.*114dup ENSP00000493056.1:n.*114dup
ENST00000641025.1:c.*114dup ENSP00000493346.1:n.*114dup
ENST00000641092.1:c.*114dup ENSP00000493392.1:n.*114dup
ENST00000641133.1:c.*543dup ENSP00000493192.1:n.*543dup
ENST00000641146.1:n.1095dup
ENST00000641147.1:c.779dup ENSP00000493133.1:p.Tyr260Ter
ENST00000641178.1:c.1094dup ENSP00000492989.1:p.Tyr365Ter
ENST00000641186.1:c.1115dup ENSP00000493347.1:p.Tyr372Ter
ENST00000641228.1:c.*114dup ENSP00000493194.1:n.*114dup
ENST00000641332.1:c.*290dup ENSP00000493397.1:n.*290dup
ENST00000641340.1:c.*358dup ENSP00000493191.1:n.*358dup
ENST00000641388.1:n.476dup
ENST00000641393.1:c.779dup ENSP00000493197.1:p.Tyr260Ter
ENST00000641397.1:c.*114dup ENSP00000493406.1:n.*114dup
ENST00000641413.1:c.154dup
ENST00000641434.1:c.1229dup ENSP00000493279.1:p.Tyr410Ter
ENST00000641464.1:c.*462dup ENSP00000493438.1:n.*462dup
ENST00000641482.1:c.*114dup ENSP00000493277.1:n.*114dup
ENST00000641508.1:c.*462dup ENSP00000493209.1:n.*462dup
ENST00000641509.1:c.914dup ENSP00000493459.1:p.Tyr305Ter
ENST00000641590.1:c.*114dup ENSP00000493132.1:n.*114dup
ENST00000641658.1:c.*394dup ENSP00000492987.1:n.*394dup
ENST00000641686.2:c.1229dup MANE Select ENSP00000493218.2:p.Tyr410Ter
ENST00000641690.1:c.1028dup ENSP00000492966.1:p.Tyr343Ter
ENST00000641742.1:c.*394dup ENSP00000493315.1:n.*394dup
ENST00000641748.1:c.1229dup ENSP00000493330.1:p.Tyr410Ter
ENST00000641753.1:c.1056dup
ENST00000641774.1:c.*481dup ENSP00000492960.1:n.*481dup
ENST00000641830.1:c.461dup
ENST00000641843.1:c.*290dup ENSP00000493174.1:n.*290dup
ENST00000641869.1:c.430dup
ENST00000641870.1:c.*290dup ENSP00000493044.1:n.*290dup
ENST00000641882.1:c.*394dup ENSP00000493301.1:n.*394dup
ENST00000641928.1:c.*358dup ENSP00000493418.1:n.*358dup
ENST00000641949.1:c.554-809dup ENSP00000492891.1:n.554-809dup
ENST00000642012.1:n.1093dup
ENST00000642034.1:c.*114dup ENSP00000493285.1:n.*114dup
ENST00000642042.1:c.1229dup ENSP00000493260.1:p.Tyr410Ter
ENST00000642078.1:c.*290dup ENSP00000492885.1:n.*290dup
ENST00000296468.7:c.1229dup ENSP00000296468.3:p.Tyr410Ter
ENST00000504126.1:n.257dup
ENST00000513559.5:c.1094dup ENSP00000425000.1:p.Tyr365Ter
ENST00000515130.5:n.1571dup
NM_152778.2:c.1229dup NP_689991.1:p.Tyr410Ter
XM_005262893.1:c.1229dup XP_005262950.1:p.Tyr410Ter
XM_005262896.1:c.1082dup XP_005262953.1:p.Tyr361Ter
XM_005262897.1:c.1028dup XP_005262954.1:p.Tyr343Ter
XM_005262898.2:c.*114dup XP_005262955.1:n.*114dup
XM_011531830.1:c.1115dup XP_011530132.1:p.Tyr372Ter
XM_011531831.1:c.914dup XP_011530133.1:p.Tyr305Ter
XM_011531832.1:c.*114dup XP_011530134.1:n.*114dup
XR_938717.1:n.1306dup
NM_001363520.1:c.1028dup NP_001350449.1:p.Tyr343Ter
NM_001363521.1:c.914dup NP_001350450.1:p.Tyr305Ter
XM_005262898.3:c.*114dup XP_005262955.1:n.*114dup
XM_017007989.1:c.*114dup XP_016863478.1:n.*114dup
XM_024453981.1:c.1094dup XP_024309749.1:p.Tyr365Ter
XM_024453982.1:c.980dup XP_024309750.1:p.Tyr327Ter
XM_024453983.1:c.779dup XP_024309751.1:p.Tyr260Ter
XR_001741194.1:n.1202dup
XR_001741195.1:n.1088dup
XR_001741196.1:n.1001dup
XR_001741197.1:n.1161dup
XR_001741198.2:n.1057dup
XR_001741199.1:n.1057dup
XR_938717.2:n.1306dup
NM_001363520.2:c.1028dup NP_001350449.1:p.Tyr343Ter
NM_001363521.2:c.914dup NP_001350450.1:p.Tyr305Ter
NM_001371590.1:c.1094dup NP_001358519.1:p.Tyr365Ter
NM_001371591.1:c.1229dup NP_001358520.1:p.Tyr410Ter
NM_001371592.1:c.1235dup NP_001358521.1:p.Tyr412Ter
NM_001371593.1:c.1115dup NP_001358522.1:p.Tyr372Ter
NM_001371594.1:c.1082dup NP_001358523.1:p.Tyr361Ter
NM_001371595.1:c.947dup NP_001358524.1:p.Tyr316Ter
NM_001371596.2:c.1229dup MANE Select NP_001358525.1:p.Tyr410Ter
NM_152778.3:c.1229dup NP_689991.1:p.Tyr410Ter
NM_152778.4:c.1229dup NP_689991.1:p.Tyr410Ter