Canonical Allele Identifier: CA2554588250
Gene: MITF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69964798_69964799insTTTAAATG , CM000665.2:g.69964798_69964799insTTTAAATG GRCh38
NC_000003.11:g.70013949_70013950insTTTAAATG , CM000665.1:g.70013949_70013950insTTTAAATG GRCh37
NC_000003.10:g.70096639_70096640insTTTAAATG NCBI36
NG_011631.1:g.230317_230318insTTTAAATG , LRG_776:g.230317_230318insTTTAAATG

Transcript Alleles

HGVS Amino-acid change
ENST00000314589.11:c.1114-49_1114-48insTTTAAATG ENSP00000324443.5:n.1114-49_1114-48insTTTAAATG
ENST00000687384.1:c.1111-49_1111-48insTTTAAATG ENSP00000510225.1:n.1111-49_1111-48insTTTAAATG
ENST00000689390.1:n.1336-49_1336-48insTTTAAATG
ENST00000693031.1:c.1087-49_1087-48insTTTAAATG ENSP00000509845.1:n.1087-49_1087-48insTTTAAATG
ENST00000693549.1:c.1114-116_1114-115insTTTAAATG ENSP00000509358.1:n.1114-116_1114-115insTTTAAATG
ENST00000314589.10:c.1114-49_1114-48insTTTAAATG ENSP00000324443.5:n.1114-49_1114-48insTTTAAATG
ENST00000352241.9:c.1180-49_1180-48insTTTAAATG MANE Select ENSP00000295600.8:n.1180-49_1180-48insTTTAAATG
ENST00000394351.9:c.859-49_859-48insTTTAAATG MANE Plus Clinical ENSP00000377880.3:n.859-49_859-48insTTTAAATG
ENST00000448226.9:c.1159-49_1159-48insTTTAAATG ENSP00000391803.3:n.1159-49_1159-48insTTTAAATG
ENST00000642352.1:c.1162-49_1162-48insTTTAAATG ENSP00000494105.1:n.1162-49_1162-48insTTTAAATG
ENST00000314557.10:c.841-49_841-48insTTTAAATG ENSP00000324246.6:n.841-49_841-48insTTTAAATG
ENST00000314589.9:c.1114-49_1114-48insTTTAAATG ENSP00000324443.5:n.1114-49_1114-48insTTTAAATG
ENST00000328528.10:c.1159-49_1159-48insTTTAAATG ENSP00000327867.6:n.1159-49_1159-48insTTTAAATG
ENST00000352241.8:c.1162-49_1162-48insTTTAAATG ENSP00000295600.7:n.1162-49_1162-48insTTTAAATG
ENST00000394351.7:c.859-49_859-48insTTTAAATG ENSP00000377880.3:n.859-49_859-48insTTTAAATG
ENST00000448226.6:c.1180-49_1180-48insTTTAAATG ENSP00000391803.2:n.1180-49_1180-48insTTTAAATG
ENST00000472437.5:c.1006-49_1006-48insTTTAAATG ENSP00000418845.1:n.1006-49_1006-48insTTTAAATG
ENST00000478490.5:c.*506-49_*506-48insTTTAAATG ENSP00000433487.1:n.*506-49_*506-48insTTTAAATG
ENST00000531774.1:c.673-49_673-48insTTTAAATG ENSP00000435909.1:n.673-49_673-48insTTTAAATG
NM_000248.3:c.859-49_859-48insTTTAAATG , LRG_776t1:c.859-49_859-48insTTTAAATG NP_000239.1:n.859-49_859-48insTTTAAATG
NM_001184967.1:c.1006-49_1006-48insTTTAAATG NP_001171896.1:n.1006-49_1006-48insTTTAAATG
NM_006722.2:c.1159-49_1159-48insTTTAAATG NP_006713.1:n.1159-49_1159-48insTTTAAATG
NM_198158.2:c.841-49_841-48insTTTAAATG NP_937801.1:n.841-49_841-48insTTTAAATG
NM_198159.2:c.1162-49_1162-48insTTTAAATG NP_937802.1:n.1162-49_1162-48insTTTAAATG
NM_198177.2:c.1114-49_1114-48insTTTAAATG NP_937820.1:n.1114-49_1114-48insTTTAAATG
NM_198178.2:c.673-49_673-48insTTTAAATG NP_937821.2:n.673-49_673-48insTTTAAATG
XM_005264754.1:c.1180-49_1180-48insTTTAAATG XP_005264811.1:n.1180-49_1180-48insTTTAAATG
XM_005264755.2:c.1132-49_1132-48insTTTAAATG XP_005264812.1:n.1132-49_1132-48insTTTAAATG
XM_006713164.2:c.1024-49_1024-48insTTTAAATG XP_006713227.1:n.1024-49_1024-48insTTTAAATG
XM_011533722.1:c.1177-49_1177-48insTTTAAATG XP_011532024.1:n.1177-49_1177-48insTTTAAATG
XM_011533723.1:c.1129-49_1129-48insTTTAAATG XP_011532025.1:n.1129-49_1129-48insTTTAAATG
XM_011533724.1:c.1024-49_1024-48insTTTAAATG XP_011532026.1:n.1024-49_1024-48insTTTAAATG
XM_011533725.1:c.1012-49_1012-48insTTTAAATG XP_011532027.1:n.1012-49_1012-48insTTTAAATG
XM_011533726.1:c.994-49_994-48insTTTAAATG XP_011532028.1:n.994-49_994-48insTTTAAATG
NM_001354604.1:c.1180-49_1180-48insTTTAAATG NP_001341533.1:n.1180-49_1180-48insTTTAAATG
NM_001354605.1:c.1177-49_1177-48insTTTAAATG NP_001341534.1:n.1177-49_1177-48insTTTAAATG
NM_001354606.1:c.1159-49_1159-48insTTTAAATG NP_001341535.1:n.1159-49_1159-48insTTTAAATG
NM_001354607.1:c.1111-49_1111-48insTTTAAATG NP_001341536.1:n.1111-49_1111-48insTTTAAATG
NM_001354608.1:c.1006-49_1006-48insTTTAAATG NP_001341537.1:n.1006-49_1006-48insTTTAAATG
NM_001184967.2:c.1006-49_1006-48insTTTAAATG NP_001171896.1:n.1006-49_1006-48insTTTAAATG
NM_001354604.2:c.1180-49_1180-48insTTTAAATG MANE Select NP_001341533.1:n.1180-49_1180-48insTTTAAATG
NM_001354605.2:c.1177-49_1177-48insTTTAAATG NP_001341534.1:n.1177-49_1177-48insTTTAAATG
NM_001354606.2:c.1159-49_1159-48insTTTAAATG NP_001341535.1:n.1159-49_1159-48insTTTAAATG
NM_001354607.2:c.1111-49_1111-48insTTTAAATG NP_001341536.1:n.1111-49_1111-48insTTTAAATG
NM_001354608.2:c.1006-49_1006-48insTTTAAATG NP_001341537.1:n.1006-49_1006-48insTTTAAATG
NM_198158.3:c.841-49_841-48insTTTAAATG NP_937801.1:n.841-49_841-48insTTTAAATG
NM_198159.3:c.1162-49_1162-48insTTTAAATG NP_937802.1:n.1162-49_1162-48insTTTAAATG
NM_198177.3:c.1114-49_1114-48insTTTAAATG NP_937820.1:n.1114-49_1114-48insTTTAAATG
NM_198178.3:c.673-49_673-48insTTTAAATG NP_937821.2:n.673-49_673-48insTTTAAATG
NM_000248.4:c.859-49_859-48insTTTAAATG MANE Plus Clinical NP_000239.1:n.859-49_859-48insTTTAAATG
NM_006722.3:c.1159-49_1159-48insTTTAAATG NP_006713.1:n.1159-49_1159-48insTTTAAATG