Canonical Allele Identifier: CA2600157742

Gene: ADAMTS3

Linked Data

• gnomAD v3: 4-72314008-G-C
• gnomAD v4: 4-72314008-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72314008G>C , CM000666.2:g.72314008G>C	GRCh38
NC_000004.11:g.73179725G>C , CM000666.1:g.73179725G>C	GRCh37
NC_000004.10:g.73398589G>C	NCBI36
NG_046955.1:g.259792C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.1600-186C>G MANE Select	ENSP00000286657.4:n.1600-186C>G
ENST00000286657.8:c.1600-186C>G	ENSP00000286657.4:n.1600-186C>G
ENST00000622135.1:c.1600-186C>G	ENSP00000480055.1:n.1600-186C>G
NM_014243.2:c.1600-186C>G	NP_055058.2:n.1600-186C>G
XM_011532421.1:c.1543-186C>G	XP_011530723.1:n.1543-186C>G
XM_011532422.1:c.1516-186C>G	XP_011530724.1:n.1516-186C>G
XM_011532423.1:c.958-186C>G	XP_011530725.1:n.958-186C>G
XM_011532424.1:c.868-186C>G	XP_011530726.1:n.868-186C>G
XM_011532421.2:c.1543-186C>G	XP_011530723.1:n.1543-186C>G
XM_011532422.3:c.1516-186C>G	XP_011530724.1:n.1516-186C>G
NM_014243.3:c.1600-186C>G MANE Select	NP_055058.2:n.1600-186C>G