Canonical Allele Identifier: CA357430697

Gene: ADAMTS3

Linked Data

• MyVariant Identifiers: chr4:g.73179394A>G (hg19) ; chr4:g.72313677A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313677A>G , CM000666.2:g.72313677A>G	GRCh38
NC_000004.11:g.73179394A>G , CM000666.1:g.73179394A>G	GRCh37
NC_000004.10:g.73398258A>G	NCBI36
NG_046955.1:g.260123T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.1745T>C MANE Select	ENSP00000286657.4:p.Met582Thr
ENST00000286657.8:c.1745T>C	ENSP00000286657.4:p.Met582Thr
ENST00000622135.1:c.1745T>C	ENSP00000480055.1:p.Met582Thr
NM_014243.2:c.1745T>C	NP_055058.2:p.Met582Thr
XM_011532421.1:c.1688T>C	XP_011530723.1:p.Met563Thr
XM_011532422.1:c.1661T>C	XP_011530724.1:p.Met554Thr
XM_011532423.1:c.1103T>C	XP_011530725.1:p.Met368Thr
XM_011532424.1:c.1013T>C	XP_011530726.1:p.Met338Thr
XM_011532421.2:c.1688T>C	XP_011530723.1:p.Met563Thr
XM_011532422.3:c.1661T>C	XP_011530724.1:p.Met554Thr
NM_014243.3:c.1745T>C MANE Select	NP_055058.2:p.Met582Thr