Canonical Allele Identifier: CA2670948888

Gene: ADAMTS3

Linked Data

• gnomAD v4: 4-72313546-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313546A>T , CM000666.2:g.72313546A>T	GRCh38
NC_000004.11:g.73179263A>T , CM000666.1:g.73179263A>T	GRCh37
NC_000004.10:g.73398127A>T	NCBI36
NG_046955.1:g.260254T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.1745+131T>A MANE Select	ENSP00000286657.4:n.1745+131T>A
ENST00000286657.8:c.1745+131T>A	ENSP00000286657.4:n.1745+131T>A
ENST00000622135.1:c.1745+131T>A	ENSP00000480055.1:n.1745+131T>A
NM_014243.2:c.1745+131T>A	NP_055058.2:n.1745+131T>A
XM_011532421.1:c.1688+131T>A	XP_011530723.1:n.1688+131T>A
XM_011532422.1:c.1661+131T>A	XP_011530724.1:n.1661+131T>A
XM_011532423.1:c.1103+131T>A	XP_011530725.1:n.1103+131T>A
XM_011532424.1:c.1013+131T>A	XP_011530726.1:n.1013+131T>A
XM_011532421.2:c.1688+131T>A	XP_011530723.1:n.1688+131T>A
XM_011532422.3:c.1661+131T>A	XP_011530724.1:n.1661+131T>A
NM_014243.3:c.1745+131T>A MANE Select	NP_055058.2:n.1745+131T>A