Canonical Allele Identifier: CA1918399688

Gene: ADAMTS14

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758130T= , CM000672.2:g.70758130T=	GRCh38
NC_000010.10:g.72517886T= , CM000672.1:g.72517886T=	GRCh37
NC_000010.9:g.72187892T=	NCBI36
NG_042147.1:g.90328T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.3067+39T= MANE Select	ENSP00000362303.1:n.3067+39T=
ENST00000373207.1:c.3067+39T=	ENSP00000362303.1:n.3067+39T=
ENST00000373208.5:c.3076+39T=	ENSP00000362304.1:n.3076+39T=
NM_080722.3:c.3067+39T=	NP_542453.2:n.3067+39T=
NM_139155.2:c.3076+39T=	NP_631894.2:n.3076+39T=
XM_011539300.1:c.2566+39T=	XP_011537602.1:n.2566+39T=
XM_011539301.1:c.2140+39T=	XP_011537603.1:n.2140+39T=
XM_011539302.1:c.2140+39T=	XP_011537604.1:n.2140+39T=
XM_011539309.1:c.1636+39T=	XP_011537611.1:n.1636+39T=
NM_080722.4:c.3067+39T= MANE Select	NP_542453.2:n.3067+39T=
NM_139155.3:c.3076+39T=	NP_631894.2:n.3076+39T=
XM_011539300.2:c.2566+39T=	XP_011537602.1:n.2566+39T=
XM_011539301.2:c.2140+39T=	XP_011537603.1:n.2140+39T=
XM_011539302.2:c.2140+39T=	XP_011537604.1:n.2140+39T=