Canonical Allele Identifier: CA434306270

Gene: MITF

Linked Data

• dbSNP Id: rs1222518599
• gnomAD v2: 3-70000991-A-C
• gnomAD v3: 3-69951840-A-C
• gnomAD v4: 3-69951840-A-C
• MyVariant Identifiers: chr3:g.70000991A>C (hg19) ; chr3:g.69951840A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69951840A>C , CM000665.2:g.69951840A>C	GRCh38
NC_000003.11:g.70000991A>C , CM000665.1:g.70000991A>C	GRCh37
NC_000003.10:g.70083681A>C	NCBI36
NG_011631.1:g.217359A>C , LRG_776:g.217359A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.843A>C	ENSP00000324443.5:p.Ala281=
ENST00000687384.1:c.840A>C	ENSP00000510225.1:p.Ala280=
ENST00000689390.1:n.1065A>C
ENST00000693031.1:c.816A>C	ENSP00000509845.1:p.Ala272=
ENST00000693549.1:c.843A>C	ENSP00000509358.1:p.Ala281=
ENST00000314589.10:c.843A>C	ENSP00000324443.5:p.Ala281=
ENST00000352241.9:c.909A>C MANE Select	ENSP00000295600.8:p.Ala303=
ENST00000394351.9:c.588A>C MANE Plus Clinical	ENSP00000377880.3:p.Ala196=
ENST00000448226.9:c.888A>C	ENSP00000391803.3:p.Ala296=
ENST00000642352.1:c.891A>C	ENSP00000494105.1:p.Ala297=
ENST00000314557.10:c.570A>C	ENSP00000324246.6:p.Ala190=
ENST00000314589.9:c.843A>C	ENSP00000324443.5:p.Ala281=
ENST00000328528.10:c.888A>C	ENSP00000327867.6:p.Ala296=
ENST00000352241.8:c.891A>C	ENSP00000295600.7:p.Ala297=
ENST00000394351.7:c.588A>C	ENSP00000377880.3:p.Ala196=
ENST00000448226.6:c.909A>C	ENSP00000391803.2:p.Ala303=
ENST00000451708.5:c.861A>C	ENSP00000398639.1:p.Ala287=
ENST00000472437.5:c.735A>C	ENSP00000418845.1:p.Ala245=
ENST00000478490.5:c.*235A>C	ENSP00000433487.1:n.*235A>C
ENST00000531774.1:c.402A>C	ENSP00000435909.1:p.Ala134=
NM_000248.3:c.588A>C , LRG_776t1:c.588A>C	NP_000239.1:p.Ala196=
NM_001184967.1:c.735A>C	NP_001171896.1:p.Ala245=
NM_006722.2:c.888A>C	NP_006713.1:p.Ala296=
NM_198158.2:c.570A>C	NP_937801.1:p.Ala190=
NM_198159.2:c.891A>C	NP_937802.1:p.Ala297=
NM_198177.2:c.843A>C	NP_937820.1:p.Ala281=
NM_198178.2:c.402A>C	NP_937821.2:p.Ala134=
XM_005264754.1:c.909A>C	XP_005264811.1:p.Ala303=
XM_005264755.2:c.861A>C	XP_005264812.1:p.Ala287=
XM_006713164.2:c.753A>C	XP_006713227.1:p.Ala251=
XM_011533722.1:c.906A>C	XP_011532024.1:p.Ala302=
XM_011533723.1:c.858A>C	XP_011532025.1:p.Ala286=
XM_011533724.1:c.753A>C	XP_011532026.1:p.Ala251=
XM_011533725.1:c.741A>C	XP_011532027.1:p.Ala247=
XM_011533726.1:c.723A>C	XP_011532028.1:p.Ala241=
NM_001354604.1:c.909A>C	NP_001341533.1:p.Ala303=
NM_001354605.1:c.906A>C	NP_001341534.1:p.Ala302=
NM_001354606.1:c.888A>C	NP_001341535.1:p.Ala296=
NM_001354607.1:c.840A>C	NP_001341536.1:p.Ala280=
NM_001354608.1:c.735A>C	NP_001341537.1:p.Ala245=
NM_001184967.2:c.735A>C	NP_001171896.1:p.Ala245=
NM_001354604.2:c.909A>C MANE Select	NP_001341533.1:p.Ala303=
NM_001354605.2:c.906A>C	NP_001341534.1:p.Ala302=
NM_001354606.2:c.888A>C	NP_001341535.1:p.Ala296=
NM_001354607.2:c.840A>C	NP_001341536.1:p.Ala280=
NM_001354608.2:c.735A>C	NP_001341537.1:p.Ala245=
NM_198158.3:c.570A>C	NP_937801.1:p.Ala190=
NM_198159.3:c.891A>C	NP_937802.1:p.Ala297=
NM_198177.3:c.843A>C	NP_937820.1:p.Ala281=
NM_198178.3:c.402A>C	NP_937821.2:p.Ala134=
NM_000248.4:c.588A>C MANE Plus Clinical	NP_000239.1:p.Ala196=
NM_006722.3:c.888A>C	NP_006713.1:p.Ala296=