Canonical Allele Identifier: CA470056202

Gene: ADAMTS14

Linked Data

• MyVariant Identifiers: chr10:g.72517762G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758006G>T , CM000672.2:g.70758006G>T	GRCh38
NC_000010.10:g.72517762G>T , CM000672.1:g.72517762G>T	GRCh37
NC_000010.9:g.72187768G>T	NCBI36
NG_042147.1:g.90204G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.2982G>T MANE Select	ENSP00000362303.1:p.Val994=
ENST00000373207.1:c.2982G>T	ENSP00000362303.1:p.Val994=
ENST00000373208.5:c.2991G>T	ENSP00000362304.1:p.Val997=
NM_080722.3:c.2982G>T	NP_542453.2:p.Val994=
NM_139155.2:c.2991G>T	NP_631894.2:p.Val997=
XM_011539300.1:c.2481G>T	XP_011537602.1:p.Val827=
XM_011539301.1:c.2055G>T	XP_011537603.1:p.Val685=
XM_011539302.1:c.2055G>T	XP_011537604.1:p.Val685=
XM_011539308.1:c.*61G>T	XP_011537610.1:n.*61G>T
XM_011539309.1:c.1551G>T	XP_011537611.1:p.Val517=
NM_080722.4:c.2982G>T MANE Select	NP_542453.2:p.Val994=
NM_139155.3:c.2991G>T	NP_631894.2:p.Val997=
XM_011539300.2:c.2481G>T	XP_011537602.1:p.Val827=
XM_011539301.2:c.2055G>T	XP_011537603.1:p.Val685=
XM_011539302.2:c.2055G>T	XP_011537604.1:p.Val685=
XM_011539308.2:c.*61G>T	XP_011537610.1:n.*61G>T