Canonical Allele Identifier: CA439879079

Gene: ADAMTS3

Linked Data

• MyVariant Identifiers: chr4:g.73179408C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313691C>T , CM000666.2:g.72313691C>T	GRCh38
NC_000004.11:g.73179408C>T , CM000666.1:g.73179408C>T	GRCh37
NC_000004.10:g.73398272C>T	NCBI36
NG_046955.1:g.260109G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.1731G>A MANE Select	ENSP00000286657.4:p.Gln577=
ENST00000286657.8:c.1731G>A	ENSP00000286657.4:p.Gln577=
ENST00000622135.1:c.1731G>A	ENSP00000480055.1:p.Gln577=
NM_014243.2:c.1731G>A	NP_055058.2:p.Gln577=
XM_011532421.1:c.1674G>A	XP_011530723.1:p.Gln558=
XM_011532422.1:c.1647G>A	XP_011530724.1:p.Gln549=
XM_011532423.1:c.1089G>A	XP_011530725.1:p.Gln363=
XM_011532424.1:c.999G>A	XP_011530726.1:p.Gln333=
XM_011532421.2:c.1674G>A	XP_011530723.1:p.Gln558=
XM_011532422.3:c.1647G>A	XP_011530724.1:p.Gln549=
NM_014243.3:c.1731G>A MANE Select	NP_055058.2:p.Gln577=