Canonical Allele Identifier: CA1467599561

Gene: ADAMTS3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313476_72313479delinsATCT , CM000666.2:g.72313476_72313479delinsATCT	GRCh38
NC_000004.11:g.73179193_73179196delinsATCT , CM000666.1:g.73179193_73179196delinsATCT	GRCh37
NC_000004.10:g.73398057_73398060delinsATCT	NCBI36
NG_046955.1:g.260321_260324delinsAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.1745+198_1745+201delinsAGAT MANE Select	ENSP00000286657.4:n.1745+198_1745+201delinsAGAT
ENST00000286657.8:c.1745+198_1745+201delinsAGAT	ENSP00000286657.4:n.1745+198_1745+201delinsAGAT
ENST00000622135.1:c.1745+198_1745+201delinsAGAT	ENSP00000480055.1:n.1745+198_1745+201delinsAGAT
NM_014243.2:c.1745+198_1745+201delinsAGAT	NP_055058.2:n.1745+198_1745+201delinsAGAT
XM_011532421.1:c.1688+198_1688+201delinsAGAT	XP_011530723.1:n.1688+198_1688+201delinsAGAT
XM_011532422.1:c.1661+198_1661+201delinsAGAT	XP_011530724.1:n.1661+198_1661+201delinsAGAT
XM_011532423.1:c.1103+198_1103+201delinsAGAT	XP_011530725.1:n.1103+198_1103+201delinsAGAT
XM_011532424.1:c.1013+198_1013+201delinsAGAT	XP_011530726.1:n.1013+198_1013+201delinsAGAT
XM_011532421.2:c.1688+198_1688+201delinsAGAT	XP_011530723.1:n.1688+198_1688+201delinsAGAT
XM_011532422.3:c.1661+198_1661+201delinsAGAT	XP_011530724.1:n.1661+198_1661+201delinsAGAT
NM_014243.3:c.1745+198_1745+201delinsAGAT MANE Select	NP_055058.2:n.1745+198_1745+201delinsAGAT