Canonical Allele Identifier: CA1918399703

Gene: ADAMTS14

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758181A= , CM000672.2:g.70758181A=	GRCh38
NC_000010.10:g.72517937A= , CM000672.1:g.72517937A=	GRCh37
NC_000010.9:g.72187943A=	NCBI36
NG_042147.1:g.90379A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.3074A= MANE Select	ENSP00000362303.1:p.His1025=
ENST00000373207.1:c.3074A=	ENSP00000362303.1:p.His1025=
ENST00000373208.5:c.3083A=	ENSP00000362304.1:p.His1028=
NM_080722.3:c.3074A=	NP_542453.2:p.His1025=
NM_139155.2:c.3083A=	NP_631894.2:p.His1028=
XM_011539300.1:c.2573A=	XP_011537602.1:p.His858=
XM_011539301.1:c.2147A=	XP_011537603.1:p.His716=
XM_011539302.1:c.2147A=	XP_011537604.1:p.His716=
XM_011539309.1:c.1643A=	XP_011537611.1:p.His548=
NM_080722.4:c.3074A= MANE Select	NP_542453.2:p.His1025=
NM_139155.3:c.3083A=	NP_631894.2:p.His1028=
XM_011539300.2:c.2573A=	XP_011537602.1:p.His858=
XM_011539301.2:c.2147A=	XP_011537603.1:p.His716=
XM_011539302.2:c.2147A=	XP_011537604.1:p.His716=