Canonical Allele Identifier: CA99549840

Gene: ADAMTS3

Linked Data

• dbSNP Id: rs990765832
• MyVariant Identifiers: chr4:g.73179235G>T (hg19) ; chr4:g.72313518G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313518G>T , CM000666.2:g.72313518G>T	GRCh38
NC_000004.11:g.73179235G>T , CM000666.1:g.73179235G>T	GRCh37
NC_000004.10:g.73398099G>T	NCBI36
NG_046955.1:g.260282C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.1745+159C>A MANE Select	ENSP00000286657.4:n.1745+159C>A
ENST00000286657.8:c.1745+159C>A	ENSP00000286657.4:n.1745+159C>A
ENST00000622135.1:c.1745+159C>A	ENSP00000480055.1:n.1745+159C>A
NM_014243.2:c.1745+159C>A	NP_055058.2:n.1745+159C>A
XM_011532421.1:c.1688+159C>A	XP_011530723.1:n.1688+159C>A
XM_011532422.1:c.1661+159C>A	XP_011530724.1:n.1661+159C>A
XM_011532423.1:c.1103+159C>A	XP_011530725.1:n.1103+159C>A
XM_011532424.1:c.1013+159C>A	XP_011530726.1:n.1013+159C>A
XM_011532421.2:c.1688+159C>A	XP_011530723.1:n.1688+159C>A
XM_011532422.3:c.1661+159C>A	XP_011530724.1:n.1661+159C>A
NM_014243.3:c.1745+159C>A MANE Select	NP_055058.2:n.1745+159C>A