Canonical Allele Identifier: CA1467599932

Gene: ADAMTS3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313769A= , CM000666.2:g.72313769A=	GRCh38
NC_000004.11:g.73179486A= , CM000666.1:g.73179486A=	GRCh37
NC_000004.10:g.73398350A=	NCBI36
NG_046955.1:g.260031T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.1653T= MANE Select	ENSP00000286657.4:p.Asp551=
ENST00000286657.8:c.1653T=	ENSP00000286657.4:p.Asp551=
ENST00000622135.1:c.1653T=	ENSP00000480055.1:p.Asp551=
NM_014243.2:c.1653T=	NP_055058.2:p.Asp551=
XM_011532421.1:c.1596T=	XP_011530723.1:p.Asp532=
XM_011532422.1:c.1569T=	XP_011530724.1:p.Asp523=
XM_011532423.1:c.1011T=	XP_011530725.1:p.Asp337=
XM_011532424.1:c.921T=	XP_011530726.1:p.Asp307=
XM_011532421.2:c.1596T=	XP_011530723.1:p.Asp532=
XM_011532422.3:c.1569T=	XP_011530724.1:p.Asp523=
NM_014243.3:c.1653T= MANE Select	NP_055058.2:p.Asp551=