Canonical Allele Identifier: CA434305910

Gene: MITF

Linked Data

• MyVariant Identifiers: chr3:g.69998297C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69949146C>T , CM000665.2:g.69949146C>T	GRCh38
NC_000003.11:g.69998297C>T , CM000665.1:g.69998297C>T	GRCh37
NC_000003.10:g.70080987C>T	NCBI36
NG_011631.1:g.214665C>T , LRG_776:g.214665C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.810C>T	ENSP00000324443.5:p.Pro270=
ENST00000687384.1:c.807C>T	ENSP00000510225.1:p.Pro269=
ENST00000689390.1:n.1032C>T
ENST00000693031.1:c.783C>T	ENSP00000509845.1:p.Pro261=
ENST00000693549.1:c.810C>T	ENSP00000509358.1:p.Pro270=
ENST00000314589.10:c.810C>T	ENSP00000324443.5:p.Pro270=
ENST00000352241.9:c.858C>T MANE Select	ENSP00000295600.8:p.Pro286=
ENST00000394351.9:c.537C>T MANE Plus Clinical	ENSP00000377880.3:p.Pro179=
ENST00000448226.9:c.855C>T	ENSP00000391803.3:p.Pro285=
ENST00000642352.1:c.858C>T	ENSP00000494105.1:p.Pro286=
ENST00000314557.10:c.537C>T	ENSP00000324246.6:p.Pro179=
ENST00000314589.9:c.810C>T	ENSP00000324443.5:p.Pro270=
ENST00000328528.10:c.855C>T	ENSP00000327867.6:p.Pro285=
ENST00000352241.8:c.858C>T	ENSP00000295600.7:p.Pro286=
ENST00000394351.7:c.537C>T	ENSP00000377880.3:p.Pro179=
ENST00000448226.6:c.858C>T	ENSP00000391803.2:p.Pro286=
ENST00000451708.5:c.810C>T	ENSP00000398639.1:p.Pro270=
ENST00000472437.5:c.702C>T	ENSP00000418845.1:p.Pro234=
ENST00000478490.5:c.*184C>T	ENSP00000433487.1:n.*184C>T
ENST00000531774.1:c.369C>T	ENSP00000435909.1:p.Pro123=
NM_000248.3:c.537C>T , LRG_776t1:c.537C>T	NP_000239.1:p.Pro179=
NM_001184967.1:c.702C>T	NP_001171896.1:p.Pro234=
NM_006722.2:c.855C>T	NP_006713.1:p.Pro285=
NM_198158.2:c.537C>T	NP_937801.1:p.Pro179=
NM_198159.2:c.858C>T	NP_937802.1:p.Pro286=
NM_198177.2:c.810C>T	NP_937820.1:p.Pro270=
NM_198178.2:c.369C>T	NP_937821.2:p.Pro123=
XM_005264754.1:c.858C>T	XP_005264811.1:p.Pro286=
XM_005264755.2:c.810C>T	XP_005264812.1:p.Pro270=
XM_006713164.2:c.702C>T	XP_006713227.1:p.Pro234=
XM_011533722.1:c.855C>T	XP_011532024.1:p.Pro285=
XM_011533723.1:c.807C>T	XP_011532025.1:p.Pro269=
XM_011533724.1:c.702C>T	XP_011532026.1:p.Pro234=
XM_011533725.1:c.690C>T	XP_011532027.1:p.Pro230=
XM_011533726.1:c.690C>T	XP_011532028.1:p.Pro230=
NM_001354604.1:c.858C>T	NP_001341533.1:p.Pro286=
NM_001354605.1:c.855C>T	NP_001341534.1:p.Pro285=
NM_001354606.1:c.855C>T	NP_001341535.1:p.Pro285=
NM_001354607.1:c.807C>T	NP_001341536.1:p.Pro269=
NM_001354608.1:c.702C>T	NP_001341537.1:p.Pro234=
NM_001184967.2:c.702C>T	NP_001171896.1:p.Pro234=
NM_001354604.2:c.858C>T MANE Select	NP_001341533.1:p.Pro286=
NM_001354605.2:c.855C>T	NP_001341534.1:p.Pro285=
NM_001354606.2:c.855C>T	NP_001341535.1:p.Pro285=
NM_001354607.2:c.807C>T	NP_001341536.1:p.Pro269=
NM_001354608.2:c.702C>T	NP_001341537.1:p.Pro234=
NM_198158.3:c.537C>T	NP_937801.1:p.Pro179=
NM_198159.3:c.858C>T	NP_937802.1:p.Pro286=
NM_198177.3:c.810C>T	NP_937820.1:p.Pro270=
NM_198178.3:c.369C>T	NP_937821.2:p.Pro123=
NM_000248.4:c.537C>T MANE Plus Clinical	NP_000239.1:p.Pro179=
NM_006722.3:c.855C>T	NP_006713.1:p.Pro285=