Canonical Allele Identifier: CA2553768583

Gene: ADAMTS3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313931_72313932insATTG , CM000666.2:g.72313931_72313932insATTG	GRCh38
NC_000004.11:g.73179648_73179649insATTG , CM000666.1:g.73179648_73179649insATTG	GRCh37
NC_000004.10:g.73398512_73398513insATTG	NCBI36
NG_046955.1:g.259868_259869insCAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.1600-110_1600-109insCAAT MANE Select	ENSP00000286657.4:n.1600-110_1600-109insCAAT
ENST00000286657.8:c.1600-110_1600-109insCAAT	ENSP00000286657.4:n.1600-110_1600-109insCAAT
ENST00000622135.1:c.1600-110_1600-109insCAAT	ENSP00000480055.1:n.1600-110_1600-109insCAAT
NM_014243.2:c.1600-110_1600-109insCAAT	NP_055058.2:n.1600-110_1600-109insCAAT
XM_011532421.1:c.1543-110_1543-109insCAAT	XP_011530723.1:n.1543-110_1543-109insCAAT
XM_011532422.1:c.1516-110_1516-109insCAAT	XP_011530724.1:n.1516-110_1516-109insCAAT
XM_011532423.1:c.958-110_958-109insCAAT	XP_011530725.1:n.958-110_958-109insCAAT
XM_011532424.1:c.868-110_868-109insCAAT	XP_011530726.1:n.868-110_868-109insCAAT
XM_011532421.2:c.1543-110_1543-109insCAAT	XP_011530723.1:n.1543-110_1543-109insCAAT
XM_011532422.3:c.1516-110_1516-109insCAAT	XP_011530724.1:n.1516-110_1516-109insCAAT
NM_014243.3:c.1600-110_1600-109insCAAT MANE Select	NP_055058.2:n.1600-110_1600-109insCAAT