Canonical Allele Identifier: CA470056205

Gene: ADAMTS14

Linked Data

• gnomAD v4: 10-70758009-C-T
• MyVariant Identifiers: chr10:g.72517765C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758009C>T , CM000672.2:g.70758009C>T	GRCh38
NC_000010.10:g.72517765C>T , CM000672.1:g.72517765C>T	GRCh37
NC_000010.9:g.72187771C>T	NCBI36
NG_042147.1:g.90207C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.2985C>T MANE Select	ENSP00000362303.1:p.Cys995=
ENST00000373207.1:c.2985C>T	ENSP00000362303.1:p.Cys995=
ENST00000373208.5:c.2994C>T	ENSP00000362304.1:p.Cys998=
NM_080722.3:c.2985C>T	NP_542453.2:p.Cys995=
NM_139155.2:c.2994C>T	NP_631894.2:p.Cys998=
XM_011539300.1:c.2484C>T	XP_011537602.1:p.Cys828=
XM_011539301.1:c.2058C>T	XP_011537603.1:p.Cys686=
XM_011539302.1:c.2058C>T	XP_011537604.1:p.Cys686=
XM_011539308.1:c.*64C>T	XP_011537610.1:n.*64C>T
XM_011539309.1:c.1554C>T	XP_011537611.1:p.Cys518=
NM_080722.4:c.2985C>T MANE Select	NP_542453.2:p.Cys995=
NM_139155.3:c.2994C>T	NP_631894.2:p.Cys998=
XM_011539300.2:c.2484C>T	XP_011537602.1:p.Cys828=
XM_011539301.2:c.2058C>T	XP_011537603.1:p.Cys686=
XM_011539302.2:c.2058C>T	XP_011537604.1:p.Cys686=
XM_011539308.2:c.*64C>T	XP_011537610.1:n.*64C>T