Canonical Allele Identifier: CA353561661

Gene: MITF

Linked Data

• ClinVar Variation Id: 1718943
• ClinVar RCV Id: RCV002301782
• MyVariant Identifiers: chr3:g.70001030C>G (hg19) ; chr3:g.69951879C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69951879C>G , CM000665.2:g.69951879C>G	GRCh38
NC_000003.11:g.70001030C>G , CM000665.1:g.70001030C>G	GRCh37
NC_000003.10:g.70083720C>G	NCBI36
NG_011631.1:g.217398C>G , LRG_776:g.217398C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.882C>G	ENSP00000324443.5:p.His294Gln
ENST00000687384.1:c.879C>G	ENSP00000510225.1:p.His293Gln
ENST00000689390.1:n.1104C>G
ENST00000693031.1:c.855C>G	ENSP00000509845.1:p.His285Gln
ENST00000693549.1:c.882C>G	ENSP00000509358.1:p.His294Gln
ENST00000314589.10:c.882C>G	ENSP00000324443.5:p.His294Gln
ENST00000352241.9:c.948C>G MANE Select	ENSP00000295600.8:p.His316Gln
ENST00000394351.9:c.627C>G MANE Plus Clinical	ENSP00000377880.3:p.His209Gln
ENST00000448226.9:c.927C>G	ENSP00000391803.3:p.His309Gln
ENST00000642352.1:c.930C>G	ENSP00000494105.1:p.His310Gln
ENST00000314557.10:c.609C>G	ENSP00000324246.6:p.His203Gln
ENST00000314589.9:c.882C>G	ENSP00000324443.5:p.His294Gln
ENST00000328528.10:c.927C>G	ENSP00000327867.6:p.His309Gln
ENST00000352241.8:c.930C>G	ENSP00000295600.7:p.His310Gln
ENST00000394351.7:c.627C>G	ENSP00000377880.3:p.His209Gln
ENST00000448226.6:c.948C>G	ENSP00000391803.2:p.His316Gln
ENST00000451708.5:c.900C>G	ENSP00000398639.1:p.His300Gln
ENST00000472437.5:c.774C>G	ENSP00000418845.1:p.His258Gln
ENST00000478490.5:c.*274C>G	ENSP00000433487.1:n.*274C>G
ENST00000531774.1:c.441C>G	ENSP00000435909.1:p.His147Gln
NM_000248.3:c.627C>G , LRG_776t1:c.627C>G	NP_000239.1:p.His209Gln
NM_001184967.1:c.774C>G	NP_001171896.1:p.His258Gln
NM_006722.2:c.927C>G	NP_006713.1:p.His309Gln
NM_198158.2:c.609C>G	NP_937801.1:p.His203Gln
NM_198159.2:c.930C>G	NP_937802.1:p.His310Gln
NM_198177.2:c.882C>G	NP_937820.1:p.His294Gln
NM_198178.2:c.441C>G	NP_937821.2:p.His147Gln
XM_005264754.1:c.948C>G	XP_005264811.1:p.His316Gln
XM_005264755.2:c.900C>G	XP_005264812.1:p.His300Gln
XM_006713164.2:c.792C>G	XP_006713227.1:p.His264Gln
XM_011533722.1:c.945C>G	XP_011532024.1:p.His315Gln
XM_011533723.1:c.897C>G	XP_011532025.1:p.His299Gln
XM_011533724.1:c.792C>G	XP_011532026.1:p.His264Gln
XM_011533725.1:c.780C>G	XP_011532027.1:p.His260Gln
XM_011533726.1:c.762C>G	XP_011532028.1:p.His254Gln
NM_001354604.1:c.948C>G	NP_001341533.1:p.His316Gln
NM_001354605.1:c.945C>G	NP_001341534.1:p.His315Gln
NM_001354606.1:c.927C>G	NP_001341535.1:p.His309Gln
NM_001354607.1:c.879C>G	NP_001341536.1:p.His293Gln
NM_001354608.1:c.774C>G	NP_001341537.1:p.His258Gln
NM_001184967.2:c.774C>G	NP_001171896.1:p.His258Gln
NM_001354604.2:c.948C>G MANE Select	NP_001341533.1:p.His316Gln
NM_001354605.2:c.945C>G	NP_001341534.1:p.His315Gln
NM_001354606.2:c.927C>G	NP_001341535.1:p.His309Gln
NM_001354607.2:c.879C>G	NP_001341536.1:p.His293Gln
NM_001354608.2:c.774C>G	NP_001341537.1:p.His258Gln
NM_198158.3:c.609C>G	NP_937801.1:p.His203Gln
NM_198159.3:c.930C>G	NP_937802.1:p.His310Gln
NM_198177.3:c.882C>G	NP_937820.1:p.His294Gln
NM_198178.3:c.441C>G	NP_937821.2:p.His147Gln
NM_000248.4:c.627C>G MANE Plus Clinical	NP_000239.1:p.His209Gln
NM_006722.3:c.927C>G	NP_006713.1:p.His309Gln