Canonical Allele Identifier: CA1918399556

Gene: ADAMTS14

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70757886C= , CM000672.2:g.70757886C=	GRCh38
NC_000010.10:g.72517642C= , CM000672.1:g.72517642C=	GRCh37
NC_000010.9:g.72187648C=	NCBI36
NG_042147.1:g.90084C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.2938-76C= MANE Select	ENSP00000362303.1:n.2938-76C=
ENST00000373207.1:c.2938-76C=	ENSP00000362303.1:n.2938-76C=
ENST00000373208.5:c.2947-76C=	ENSP00000362304.1:n.2947-76C=
NM_080722.3:c.2938-76C=	NP_542453.2:n.2938-76C=
NM_139155.2:c.2947-76C=	NP_631894.2:n.2947-76C=
XM_011539300.1:c.2437-76C=	XP_011537602.1:n.2437-76C=
XM_011539301.1:c.2011-76C=	XP_011537603.1:n.2011-76C=
XM_011539302.1:c.2011-76C=	XP_011537604.1:n.2011-76C=
XM_011539308.1:c.*17-76C=	XP_011537610.1:n.*17-76C=
XM_011539309.1:c.1507-76C=	XP_011537611.1:n.1507-76C=
NM_080722.4:c.2938-76C= MANE Select	NP_542453.2:n.2938-76C=
NM_139155.3:c.2947-76C=	NP_631894.2:n.2947-76C=
XM_011539300.2:c.2437-76C=	XP_011537602.1:n.2437-76C=
XM_011539301.2:c.2011-76C=	XP_011537603.1:n.2011-76C=
XM_011539302.2:c.2011-76C=	XP_011537604.1:n.2011-76C=
XM_011539308.2:c.*17-76C=	XP_011537610.1:n.*17-76C=