Canonical Allele Identifier: CA2670948934

Gene: ADAMTS3

Linked Data

• gnomAD v4: 4-72313654-AAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313657_72313658del , CM000666.2:g.72313657_72313658del	GRCh38
NC_000004.11:g.73179374_73179375del , CM000666.1:g.73179374_73179375del	GRCh37
NC_000004.10:g.73398238_73398239del	NCBI36
NG_046955.1:g.260144_260145del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.1745+21_1745+22del MANE Select	ENSP00000286657.4:n.1745+21_1745+22del
ENST00000286657.8:c.1745+21_1745+22del	ENSP00000286657.4:n.1745+21_1745+22del
ENST00000622135.1:c.1745+21_1745+22del	ENSP00000480055.1:n.1745+21_1745+22del
NM_014243.2:c.1745+21_1745+22del	NP_055058.2:n.1745+21_1745+22del
XM_011532421.1:c.1688+21_1688+22del	XP_011530723.1:n.1688+21_1688+22del
XM_011532422.1:c.1661+21_1661+22del	XP_011530724.1:n.1661+21_1661+22del
XM_011532423.1:c.1103+21_1103+22del	XP_011530725.1:n.1103+21_1103+22del
XM_011532424.1:c.1013+21_1013+22del	XP_011530726.1:n.1013+21_1013+22del
XM_011532421.2:c.1688+21_1688+22del	XP_011530723.1:n.1688+21_1688+22del
XM_011532422.3:c.1661+21_1661+22del	XP_011530724.1:n.1661+21_1661+22del
NM_014243.3:c.1745+21_1745+22del MANE Select	NP_055058.2:n.1745+21_1745+22del