Canonical Allele Identifier: CA377108816

Gene: ADAMTS14

Linked Data

• gnomAD v4: 10-70757983-G-C
• MyVariant Identifiers: chr10:g.72517739G>C (hg19) ; chr10:g.70757983G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70757983G>C , CM000672.2:g.70757983G>C	GRCh38
NC_000010.10:g.72517739G>C , CM000672.1:g.72517739G>C	GRCh37
NC_000010.9:g.72187745G>C	NCBI36
NG_042147.1:g.90181G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.2959G>C MANE Select	ENSP00000362303.1:p.Gly987Arg
ENST00000373207.1:c.2959G>C	ENSP00000362303.1:p.Gly987Arg
ENST00000373208.5:c.2968G>C	ENSP00000362304.1:p.Gly990Arg
NM_080722.3:c.2959G>C	NP_542453.2:p.Gly987Arg
NM_139155.2:c.2968G>C	NP_631894.2:p.Gly990Arg
XM_011539300.1:c.2458G>C	XP_011537602.1:p.Gly820Arg
XM_011539301.1:c.2032G>C	XP_011537603.1:p.Gly678Arg
XM_011539302.1:c.2032G>C	XP_011537604.1:p.Gly678Arg
XM_011539308.1:c.*38G>C	XP_011537610.1:n.*38G>C
XM_011539309.1:c.1528G>C	XP_011537611.1:p.Gly510Arg
NM_080722.4:c.2959G>C MANE Select	NP_542453.2:p.Gly987Arg
NM_139155.3:c.2968G>C	NP_631894.2:p.Gly990Arg
XM_011539300.2:c.2458G>C	XP_011537602.1:p.Gly820Arg
XM_011539301.2:c.2032G>C	XP_011537603.1:p.Gly678Arg
XM_011539302.2:c.2032G>C	XP_011537604.1:p.Gly678Arg
XM_011539308.2:c.*38G>C	XP_011537610.1:n.*38G>C