Canonical Allele Identifier: CA434433785

Gene: MITF

Linked Data

• gnomAD v4: 3-69965089-C-T
• MyVariant Identifiers: chr3:g.70014240C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69965089C>T , CM000665.2:g.69965089C>T	GRCh38
NC_000003.11:g.70014240C>T , CM000665.1:g.70014240C>T	GRCh37
NC_000003.10:g.70096930C>T	NCBI36
NG_011631.1:g.230608C>T , LRG_776:g.230608C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.1356C>T	ENSP00000324443.5:p.Pro452=
ENST00000687384.1:c.1353C>T	ENSP00000510225.1:p.Pro451=
ENST00000689390.1:n.1578C>T
ENST00000693031.1:c.1329C>T	ENSP00000509845.1:p.Pro443=
ENST00000693549.1:c.*167C>T	ENSP00000509358.1:n.*167C>T
ENST00000314589.10:c.1356C>T	ENSP00000324443.5:p.Pro452=
ENST00000352241.9:c.1422C>T MANE Select	ENSP00000295600.8:p.Pro474=
ENST00000394351.9:c.1101C>T MANE Plus Clinical	ENSP00000377880.3:p.Pro367=
ENST00000448226.9:c.1401C>T	ENSP00000391803.3:p.Pro467=
ENST00000642352.1:c.1404C>T	ENSP00000494105.1:p.Pro468=
ENST00000314557.10:c.1083C>T	ENSP00000324246.6:p.Pro361=
ENST00000314589.9:c.1356C>T	ENSP00000324443.5:p.Pro452=
ENST00000328528.10:c.1401C>T	ENSP00000327867.6:p.Pro467=
ENST00000352241.8:c.1404C>T	ENSP00000295600.7:p.Pro468=
ENST00000394351.7:c.1101C>T	ENSP00000377880.3:p.Pro367=
ENST00000448226.6:c.1422C>T	ENSP00000391803.2:p.Pro474=
ENST00000472437.5:c.1248C>T	ENSP00000418845.1:p.Pro416=
ENST00000478490.5:c.*748C>T	ENSP00000433487.1:n.*748C>T
ENST00000531774.1:c.915C>T	ENSP00000435909.1:p.Pro305=
NM_000248.3:c.1101C>T , LRG_776t1:c.1101C>T	NP_000239.1:p.Pro367=
NM_001184967.1:c.1248C>T	NP_001171896.1:p.Pro416=
NM_006722.2:c.1401C>T	NP_006713.1:p.Pro467=
NM_198158.2:c.1083C>T	NP_937801.1:p.Pro361=
NM_198159.2:c.1404C>T	NP_937802.1:p.Pro468=
NM_198177.2:c.1356C>T	NP_937820.1:p.Pro452=
NM_198178.2:c.915C>T	NP_937821.2:p.Pro305=
XM_005264754.1:c.1422C>T	XP_005264811.1:p.Pro474=
XM_005264755.2:c.1374C>T	XP_005264812.1:p.Pro458=
XM_006713164.2:c.1266C>T	XP_006713227.1:p.Pro422=
XM_011533722.1:c.1419C>T	XP_011532024.1:p.Pro473=
XM_011533723.1:c.1371C>T	XP_011532025.1:p.Pro457=
XM_011533724.1:c.1266C>T	XP_011532026.1:p.Pro422=
XM_011533725.1:c.1254C>T	XP_011532027.1:p.Pro418=
XM_011533726.1:c.1236C>T	XP_011532028.1:p.Pro412=
NM_001354604.1:c.1422C>T	NP_001341533.1:p.Pro474=
NM_001354605.1:c.1419C>T	NP_001341534.1:p.Pro473=
NM_001354606.1:c.1401C>T	NP_001341535.1:p.Pro467=
NM_001354607.1:c.1353C>T	NP_001341536.1:p.Pro451=
NM_001354608.1:c.1248C>T	NP_001341537.1:p.Pro416=
NM_001184967.2:c.1248C>T	NP_001171896.1:p.Pro416=
NM_001354604.2:c.1422C>T MANE Select	NP_001341533.1:p.Pro474=
NM_001354605.2:c.1419C>T	NP_001341534.1:p.Pro473=
NM_001354606.2:c.1401C>T	NP_001341535.1:p.Pro467=
NM_001354607.2:c.1353C>T	NP_001341536.1:p.Pro451=
NM_001354608.2:c.1248C>T	NP_001341537.1:p.Pro416=
NM_198158.3:c.1083C>T	NP_937801.1:p.Pro361=
NM_198159.3:c.1404C>T	NP_937802.1:p.Pro468=
NM_198177.3:c.1356C>T	NP_937820.1:p.Pro452=
NM_198178.3:c.915C>T	NP_937821.2:p.Pro305=
NM_000248.4:c.1101C>T MANE Plus Clinical	NP_000239.1:p.Pro367=
NM_006722.3:c.1401C>T	NP_006713.1:p.Pro467=