Canonical Allele Identifier: CA357430778

Gene: ADAMTS3

Linked Data

• MyVariant Identifiers: chr4:g.73179433G>T (hg19) ; chr4:g.72313716G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313716G>T , CM000666.2:g.72313716G>T	GRCh38
NC_000004.11:g.73179433G>T , CM000666.1:g.73179433G>T	GRCh37
NC_000004.10:g.73398297G>T	NCBI36
NG_046955.1:g.260084C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.1706C>A MANE Select	ENSP00000286657.4:p.Thr569Asn
ENST00000286657.8:c.1706C>A	ENSP00000286657.4:p.Thr569Asn
ENST00000622135.1:c.1706C>A	ENSP00000480055.1:p.Thr569Asn
NM_014243.2:c.1706C>A	NP_055058.2:p.Thr569Asn
XM_011532421.1:c.1649C>A	XP_011530723.1:p.Thr550Asn
XM_011532422.1:c.1622C>A	XP_011530724.1:p.Thr541Asn
XM_011532423.1:c.1064C>A	XP_011530725.1:p.Thr355Asn
XM_011532424.1:c.974C>A	XP_011530726.1:p.Thr325Asn
XM_011532421.2:c.1649C>A	XP_011530723.1:p.Thr550Asn
XM_011532422.3:c.1622C>A	XP_011530724.1:p.Thr541Asn
NM_014243.3:c.1706C>A MANE Select	NP_055058.2:p.Thr569Asn