Canonical Allele Identifier: CA1918399655

Gene: ADAMTS14

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758055G= , CM000672.2:g.70758055G=	GRCh38
NC_000010.10:g.72517811G= , CM000672.1:g.72517811G=	GRCh37
NC_000010.9:g.72187817G=	NCBI36
NG_042147.1:g.90253G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.3031G= MANE Select	ENSP00000362303.1:p.Asp1011=
ENST00000373207.1:c.3031G=	ENSP00000362303.1:p.Asp1011=
ENST00000373208.5:c.3040G=	ENSP00000362304.1:p.Asp1014=
NM_080722.3:c.3031G=	NP_542453.2:p.Asp1011=
NM_139155.2:c.3040G=	NP_631894.2:p.Asp1014=
XM_011539300.1:c.2530G=	XP_011537602.1:p.Asp844=
XM_011539301.1:c.2104G=	XP_011537603.1:p.Asp702=
XM_011539302.1:c.2104G=	XP_011537604.1:p.Asp702=
XM_011539309.1:c.1600G=	XP_011537611.1:p.Asp534=
NM_080722.4:c.3031G= MANE Select	NP_542453.2:p.Asp1011=
NM_139155.3:c.3040G=	NP_631894.2:p.Asp1014=
XM_011539300.2:c.2530G=	XP_011537602.1:p.Asp844=
XM_011539301.2:c.2104G=	XP_011537603.1:p.Asp702=
XM_011539302.2:c.2104G=	XP_011537604.1:p.Asp702=