Canonical Allele Identifier: CA357430780

Gene: ADAMTS3

Linked Data

• MyVariant Identifiers: chr4:g.73179434T>C (hg19) ; chr4:g.72313717T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313717T>C , CM000666.2:g.72313717T>C	GRCh38
NC_000004.11:g.73179434T>C , CM000666.1:g.73179434T>C	GRCh37
NC_000004.10:g.73398298T>C	NCBI36
NG_046955.1:g.260083A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.1705A>G MANE Select	ENSP00000286657.4:p.Thr569Ala
ENST00000286657.8:c.1705A>G	ENSP00000286657.4:p.Thr569Ala
ENST00000622135.1:c.1705A>G	ENSP00000480055.1:p.Thr569Ala
NM_014243.2:c.1705A>G	NP_055058.2:p.Thr569Ala
XM_011532421.1:c.1648A>G	XP_011530723.1:p.Thr550Ala
XM_011532422.1:c.1621A>G	XP_011530724.1:p.Thr541Ala
XM_011532423.1:c.1063A>G	XP_011530725.1:p.Thr355Ala
XM_011532424.1:c.973A>G	XP_011530726.1:p.Thr325Ala
XM_011532421.2:c.1648A>G	XP_011530723.1:p.Thr550Ala
XM_011532422.3:c.1621A>G	XP_011530724.1:p.Thr541Ala
NM_014243.3:c.1705A>G MANE Select	NP_055058.2:p.Thr569Ala