Canonical Allele Identifier: CA1918399648

Gene: ADAMTS14

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758040G= , CM000672.2:g.70758040G=	GRCh38
NC_000010.10:g.72517796G= , CM000672.1:g.72517796G=	GRCh37
NC_000010.9:g.72187802G=	NCBI36
NG_042147.1:g.90238G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.3016G= MANE Select	ENSP00000362303.1:p.Glu1006=
ENST00000373207.1:c.3016G=	ENSP00000362303.1:p.Glu1006=
ENST00000373208.5:c.3025G=	ENSP00000362304.1:p.Glu1009=
NM_080722.3:c.3016G=	NP_542453.2:p.Glu1006=
NM_139155.2:c.3025G=	NP_631894.2:p.Glu1009=
XM_011539300.1:c.2515G=	XP_011537602.1:p.Glu839=
XM_011539301.1:c.2089G=	XP_011537603.1:p.Glu697=
XM_011539302.1:c.2089G=	XP_011537604.1:p.Glu697=
XM_011539309.1:c.1585G=	XP_011537611.1:p.Glu529=
NM_080722.4:c.3016G= MANE Select	NP_542453.2:p.Glu1006=
NM_139155.3:c.3025G=	NP_631894.2:p.Glu1009=
XM_011539300.2:c.2515G=	XP_011537602.1:p.Glu839=
XM_011539301.2:c.2089G=	XP_011537603.1:p.Glu697=
XM_011539302.2:c.2089G=	XP_011537604.1:p.Glu697=
XM_011539308.2:c.*95G=	XP_011537610.1:n.*95G=