Canonical Allele Identifier: CA213179

Gene: MITF

Linked Data

• ClinVar Variation Id: 14275
• ClinVar RCV Id: RCV000015345
• dbSNP Id: rs104893745
• MyVariant Identifiers: chr3:g.70001033C>G (hg19) ; chr3:g.69951882C>G (hg38)
• PubMed: PMID:10851256 ; PMID:13985019

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69951882C>G , CM000665.2:g.69951882C>G	GRCh38
NC_000003.11:g.70001033C>G , CM000665.1:g.70001033C>G	GRCh37
NC_000003.10:g.70083723C>G	NCBI36
NG_011631.1:g.217401C>G , LRG_776:g.217401C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.885C>G	ENSP00000324443.5:p.Asn295Lys
ENST00000687384.1:c.882C>G	ENSP00000510225.1:p.Asn294Lys
ENST00000689390.1:n.1107C>G
ENST00000693031.1:c.858C>G	ENSP00000509845.1:p.Asn286Lys
ENST00000693549.1:c.885C>G	ENSP00000509358.1:p.Asn295Lys
ENST00000314589.10:c.885C>G	ENSP00000324443.5:p.Asn295Lys
ENST00000352241.9:c.951C>G MANE Select	ENSP00000295600.8:p.Asn317Lys
ENST00000394351.9:c.630C>G MANE Plus Clinical	ENSP00000377880.3:p.Asn210Lys
ENST00000448226.9:c.930C>G	ENSP00000391803.3:p.Asn310Lys
ENST00000642352.1:c.933C>G	ENSP00000494105.1:p.Asn311Lys
ENST00000314557.10:c.612C>G	ENSP00000324246.6:p.Asn204Lys
ENST00000314589.9:c.885C>G	ENSP00000324443.5:p.Asn295Lys
ENST00000328528.10:c.930C>G	ENSP00000327867.6:p.Asn310Lys
ENST00000352241.8:c.933C>G	ENSP00000295600.7:p.Asn311Lys
ENST00000394351.7:c.630C>G	ENSP00000377880.3:p.Asn210Lys
ENST00000448226.6:c.951C>G	ENSP00000391803.2:p.Asn317Lys
ENST00000451708.5:c.903C>G	ENSP00000398639.1:p.Asn301Lys
ENST00000472437.5:c.777C>G	ENSP00000418845.1:p.Asn259Lys
ENST00000478490.5:c.*277C>G	ENSP00000433487.1:n.*277C>G
ENST00000531774.1:c.444C>G	ENSP00000435909.1:p.Asn148Lys
NM_000248.3:c.630C>G , LRG_776t1:c.630C>G	NP_000239.1:p.Asn210Lys
NM_001184967.1:c.777C>G	NP_001171896.1:p.Asn259Lys
NM_006722.2:c.930C>G	NP_006713.1:p.Asn310Lys
NM_198158.2:c.612C>G	NP_937801.1:p.Asn204Lys
NM_198159.2:c.933C>G	NP_937802.1:p.Asn311Lys
NM_198177.2:c.885C>G	NP_937820.1:p.Asn295Lys
NM_198178.2:c.444C>G	NP_937821.2:p.Asn148Lys
XM_005264754.1:c.951C>G	XP_005264811.1:p.Asn317Lys
XM_005264755.2:c.903C>G	XP_005264812.1:p.Asn301Lys
XM_006713164.2:c.795C>G	XP_006713227.1:p.Asn265Lys
XM_011533722.1:c.948C>G	XP_011532024.1:p.Asn316Lys
XM_011533723.1:c.900C>G	XP_011532025.1:p.Asn300Lys
XM_011533724.1:c.795C>G	XP_011532026.1:p.Asn265Lys
XM_011533725.1:c.783C>G	XP_011532027.1:p.Asn261Lys
XM_011533726.1:c.765C>G	XP_011532028.1:p.Asn255Lys
NM_001354604.1:c.951C>G	NP_001341533.1:p.Asn317Lys
NM_001354605.1:c.948C>G	NP_001341534.1:p.Asn316Lys
NM_001354606.1:c.930C>G	NP_001341535.1:p.Asn310Lys
NM_001354607.1:c.882C>G	NP_001341536.1:p.Asn294Lys
NM_001354608.1:c.777C>G	NP_001341537.1:p.Asn259Lys
NM_001184967.2:c.777C>G	NP_001171896.1:p.Asn259Lys
NM_001354604.2:c.951C>G MANE Select	NP_001341533.1:p.Asn317Lys
NM_001354605.2:c.948C>G	NP_001341534.1:p.Asn316Lys
NM_001354606.2:c.930C>G	NP_001341535.1:p.Asn310Lys
NM_001354607.2:c.882C>G	NP_001341536.1:p.Asn294Lys
NM_001354608.2:c.777C>G	NP_001341537.1:p.Asn259Lys
NM_198158.3:c.612C>G	NP_937801.1:p.Asn204Lys
NM_198159.3:c.933C>G	NP_937802.1:p.Asn311Lys
NM_198177.3:c.885C>G	NP_937820.1:p.Asn295Lys
NM_198178.3:c.444C>G	NP_937821.2:p.Asn148Lys
NM_000248.4:c.630C>G MANE Plus Clinical	NP_000239.1:p.Asn210Lys
NM_006722.3:c.930C>G	NP_006713.1:p.Asn310Lys