Canonical Allele Identifier: CA353559969

Gene: MITF

Linked Data

• MyVariant Identifiers: chr3:g.70014317T>C (hg19) ; chr3:g.69965166T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69965166T>C , CM000665.2:g.69965166T>C	GRCh38
NC_000003.11:g.70014317T>C , CM000665.1:g.70014317T>C	GRCh37
NC_000003.10:g.70097007T>C	NCBI36
NG_011631.1:g.230685T>C , LRG_776:g.230685T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.1433T>C	ENSP00000324443.5:p.Leu478Pro
ENST00000687384.1:c.1430T>C	ENSP00000510225.1:p.Leu477Pro
ENST00000689390.1:n.1655T>C
ENST00000693031.1:c.1406T>C	ENSP00000509845.1:p.Leu469Pro
ENST00000693549.1:c.*244T>C	ENSP00000509358.1:n.*244T>C
ENST00000314589.10:c.1433T>C	ENSP00000324443.5:p.Leu478Pro
ENST00000352241.9:c.1499T>C MANE Select	ENSP00000295600.8:p.Leu500Pro
ENST00000394351.9:c.1178T>C MANE Plus Clinical	ENSP00000377880.3:p.Leu393Pro
ENST00000448226.9:c.1478T>C	ENSP00000391803.3:p.Leu493Pro
ENST00000642352.1:c.1481T>C	ENSP00000494105.1:p.Leu494Pro
ENST00000314557.10:c.1160T>C	ENSP00000324246.6:p.Leu387Pro
ENST00000314589.9:c.1433T>C	ENSP00000324443.5:p.Leu478Pro
ENST00000328528.10:c.1478T>C	ENSP00000327867.6:p.Leu493Pro
ENST00000352241.8:c.1481T>C	ENSP00000295600.7:p.Leu494Pro
ENST00000394351.7:c.1178T>C	ENSP00000377880.3:p.Leu393Pro
ENST00000448226.6:c.1499T>C	ENSP00000391803.2:p.Leu500Pro
ENST00000472437.5:c.1325T>C	ENSP00000418845.1:p.Leu442Pro
ENST00000478490.5:c.*825T>C	ENSP00000433487.1:n.*825T>C
ENST00000531774.1:c.992T>C	ENSP00000435909.1:p.Leu331Pro
NM_000248.3:c.1178T>C , LRG_776t1:c.1178T>C	NP_000239.1:p.Leu393Pro
NM_001184967.1:c.1325T>C	NP_001171896.1:p.Leu442Pro
NM_006722.2:c.1478T>C	NP_006713.1:p.Leu493Pro
NM_198158.2:c.1160T>C	NP_937801.1:p.Leu387Pro
NM_198159.2:c.1481T>C	NP_937802.1:p.Leu494Pro
NM_198177.2:c.1433T>C	NP_937820.1:p.Leu478Pro
NM_198178.2:c.992T>C	NP_937821.2:p.Leu331Pro
XM_005264754.1:c.1499T>C	XP_005264811.1:p.Leu500Pro
XM_005264755.2:c.1451T>C	XP_005264812.1:p.Leu484Pro
XM_006713164.2:c.1343T>C	XP_006713227.1:p.Leu448Pro
XM_011533722.1:c.1496T>C	XP_011532024.1:p.Leu499Pro
XM_011533723.1:c.1448T>C	XP_011532025.1:p.Leu483Pro
XM_011533724.1:c.1343T>C	XP_011532026.1:p.Leu448Pro
XM_011533725.1:c.1331T>C	XP_011532027.1:p.Leu444Pro
XM_011533726.1:c.1313T>C	XP_011532028.1:p.Leu438Pro
NM_001354604.1:c.1499T>C	NP_001341533.1:p.Leu500Pro
NM_001354605.1:c.1496T>C	NP_001341534.1:p.Leu499Pro
NM_001354606.1:c.1478T>C	NP_001341535.1:p.Leu493Pro
NM_001354607.1:c.1430T>C	NP_001341536.1:p.Leu477Pro
NM_001354608.1:c.1325T>C	NP_001341537.1:p.Leu442Pro
NM_001184967.2:c.1325T>C	NP_001171896.1:p.Leu442Pro
NM_001354604.2:c.1499T>C MANE Select	NP_001341533.1:p.Leu500Pro
NM_001354605.2:c.1496T>C	NP_001341534.1:p.Leu499Pro
NM_001354606.2:c.1478T>C	NP_001341535.1:p.Leu493Pro
NM_001354607.2:c.1430T>C	NP_001341536.1:p.Leu477Pro
NM_001354608.2:c.1325T>C	NP_001341537.1:p.Leu442Pro
NM_198158.3:c.1160T>C	NP_937801.1:p.Leu387Pro
NM_198159.3:c.1481T>C	NP_937802.1:p.Leu494Pro
NM_198177.3:c.1433T>C	NP_937820.1:p.Leu478Pro
NM_198178.3:c.992T>C	NP_937821.2:p.Leu331Pro
NM_000248.4:c.1178T>C MANE Plus Clinical	NP_000239.1:p.Leu393Pro
NM_006722.3:c.1478T>C	NP_006713.1:p.Leu493Pro