Canonical Allele Identifier: CA1049249885

Gene: MITF

Linked Data

• dbSNP Id: rs2066396503
• gnomAD v4: 3-69956327-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69956332del , CM000665.2:g.69956332del	GRCh38
NC_000003.11:g.70005483del , CM000665.1:g.70005483del	GRCh37
NC_000003.10:g.70088173del	NCBI36
NG_011631.1:g.221851del , LRG_776:g.221851del

Transcript Alleles

HGVS	Amino-acid change
ENST00000314589.11:c.890-123del	ENSP00000324443.5:n.890-123del
ENST00000687384.1:c.887-123del	ENSP00000510225.1:n.887-123del
ENST00000689390.1:n.1112-123del
ENST00000693031.1:c.863-123del	ENSP00000509845.1:n.863-123del
ENST00000693549.1:c.890-123del	ENSP00000509358.1:n.890-123del
ENST00000314589.10:c.890-123del	ENSP00000324443.5:n.890-123del
ENST00000352241.9:c.956-123del MANE Select	ENSP00000295600.8:n.956-123del
ENST00000394351.9:c.635-123del MANE Plus Clinical	ENSP00000377880.3:n.635-123del
ENST00000448226.9:c.935-123del	ENSP00000391803.3:n.935-123del
ENST00000642352.1:c.938-123del	ENSP00000494105.1:n.938-123del
ENST00000314557.10:c.617-123del	ENSP00000324246.6:n.617-123del
ENST00000314589.9:c.890-123del	ENSP00000324443.5:n.890-123del
ENST00000328528.10:c.935-123del	ENSP00000327867.6:n.935-123del
ENST00000352241.8:c.938-123del	ENSP00000295600.7:n.938-123del
ENST00000394351.7:c.635-123del	ENSP00000377880.3:n.635-123del
ENST00000448226.6:c.956-123del	ENSP00000391803.2:n.956-123del
ENST00000451708.5:c.908-123del	ENSP00000398639.1:n.908-123del
ENST00000472437.5:c.782-123del	ENSP00000418845.1:n.782-123del
ENST00000478490.5:c.*282-123del	ENSP00000433487.1:n.*282-123del
ENST00000531774.1:c.449-123del	ENSP00000435909.1:n.449-123del
NM_000248.3:c.635-123del , LRG_776t1:c.635-123del	NP_000239.1:n.635-123del
NM_001184967.1:c.782-123del	NP_001171896.1:n.782-123del
NM_006722.2:c.935-123del	NP_006713.1:n.935-123del
NM_198158.2:c.617-123del	NP_937801.1:n.617-123del
NM_198159.2:c.938-123del	NP_937802.1:n.938-123del
NM_198177.2:c.890-123del	NP_937820.1:n.890-123del
NM_198178.2:c.449-123del	NP_937821.2:n.449-123del
XM_005264754.1:c.956-123del	XP_005264811.1:n.956-123del
XM_005264755.2:c.908-123del	XP_005264812.1:n.908-123del
XM_006713164.2:c.800-123del	XP_006713227.1:n.800-123del
XM_011533722.1:c.953-123del	XP_011532024.1:n.953-123del
XM_011533723.1:c.905-123del	XP_011532025.1:n.905-123del
XM_011533724.1:c.800-123del	XP_011532026.1:n.800-123del
XM_011533725.1:c.788-123del	XP_011532027.1:n.788-123del
XM_011533726.1:c.770-123del	XP_011532028.1:n.770-123del
NM_001354604.1:c.956-123del	NP_001341533.1:n.956-123del
NM_001354605.1:c.953-123del	NP_001341534.1:n.953-123del
NM_001354606.1:c.935-123del	NP_001341535.1:n.935-123del
NM_001354607.1:c.887-123del	NP_001341536.1:n.887-123del
NM_001354608.1:c.782-123del	NP_001341537.1:n.782-123del
NM_001184967.2:c.782-123del	NP_001171896.1:n.782-123del
NM_001354604.2:c.956-123del MANE Select	NP_001341533.1:n.956-123del
NM_001354605.2:c.953-123del	NP_001341534.1:n.953-123del
NM_001354606.2:c.935-123del	NP_001341535.1:n.935-123del
NM_001354607.2:c.887-123del	NP_001341536.1:n.887-123del
NM_001354608.2:c.782-123del	NP_001341537.1:n.782-123del
NM_198158.3:c.617-123del	NP_937801.1:n.617-123del
NM_198159.3:c.938-123del	NP_937802.1:n.938-123del
NM_198177.3:c.890-123del	NP_937820.1:n.890-123del
NM_198178.3:c.449-123del	NP_937821.2:n.449-123del
NM_000248.4:c.635-123del MANE Plus Clinical	NP_000239.1:n.635-123del
NM_006722.3:c.935-123del	NP_006713.1:n.935-123del