Canonical Allele Identifier: CA470056258

Gene: ADAMTS14

Linked Data

• gnomAD v4: 10-70758069-C-A
• MyVariant Identifiers: chr10:g.72517825C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758069C>A , CM000672.2:g.70758069C>A	GRCh38
NC_000010.10:g.72517825C>A , CM000672.1:g.72517825C>A	GRCh37
NC_000010.9:g.72187831C>A	NCBI36
NG_042147.1:g.90267C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.3045C>A MANE Select	ENSP00000362303.1:p.Val1015=
ENST00000373207.1:c.3045C>A	ENSP00000362303.1:p.Val1015=
ENST00000373208.5:c.3054C>A	ENSP00000362304.1:p.Val1018=
NM_080722.3:c.3045C>A	NP_542453.2:p.Val1015=
NM_139155.2:c.3054C>A	NP_631894.2:p.Val1018=
XM_011539300.1:c.2544C>A	XP_011537602.1:p.Val848=
XM_011539301.1:c.2118C>A	XP_011537603.1:p.Val706=
XM_011539302.1:c.2118C>A	XP_011537604.1:p.Val706=
XM_011539309.1:c.1614C>A	XP_011537611.1:p.Val538=
NM_080722.4:c.3045C>A MANE Select	NP_542453.2:p.Val1015=
NM_139155.3:c.3054C>A	NP_631894.2:p.Val1018=
XM_011539300.2:c.2544C>A	XP_011537602.1:p.Val848=
XM_011539301.2:c.2118C>A	XP_011537603.1:p.Val706=
XM_011539302.2:c.2118C>A	XP_011537604.1:p.Val706=