Canonical Allele Identifier: CA1467599895

Gene: ADAMTS3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313749G= , CM000666.2:g.72313749G=	GRCh38
NC_000004.11:g.73179466G= , CM000666.1:g.73179466G=	GRCh37
NC_000004.10:g.73398330G=	NCBI36
NG_046955.1:g.260051C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.1673C= MANE Select	ENSP00000286657.4:p.Thr558=
ENST00000286657.8:c.1673C=	ENSP00000286657.4:p.Thr558=
ENST00000622135.1:c.1673C=	ENSP00000480055.1:p.Thr558=
NM_014243.2:c.1673C=	NP_055058.2:p.Thr558=
XM_011532421.1:c.1616C=	XP_011530723.1:p.Thr539=
XM_011532422.1:c.1589C=	XP_011530724.1:p.Thr530=
XM_011532423.1:c.1031C=	XP_011530725.1:p.Thr344=
XM_011532424.1:c.941C=	XP_011530726.1:p.Thr314=
XM_011532421.2:c.1616C=	XP_011530723.1:p.Thr539=
XM_011532422.3:c.1589C=	XP_011530724.1:p.Thr530=
NM_014243.3:c.1673C= MANE Select	NP_055058.2:p.Thr558=