Canonical Allele Identifier: CA1918399702

Gene: ADAMTS14

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758177A= , CM000672.2:g.70758177A=	GRCh38
NC_000010.10:g.72517933A= , CM000672.1:g.72517933A=	GRCh37
NC_000010.9:g.72187939A=	NCBI36
NG_042147.1:g.90375A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.3070A= MANE Select	ENSP00000362303.1:p.Asn1024=
ENST00000373207.1:c.3070A=	ENSP00000362303.1:p.Asn1024=
ENST00000373208.5:c.3079A=	ENSP00000362304.1:p.Asn1027=
NM_080722.3:c.3070A=	NP_542453.2:p.Asn1024=
NM_139155.2:c.3079A=	NP_631894.2:p.Asn1027=
XM_011539300.1:c.2569A=	XP_011537602.1:p.Asn857=
XM_011539301.1:c.2143A=	XP_011537603.1:p.Asn715=
XM_011539302.1:c.2143A=	XP_011537604.1:p.Asn715=
XM_011539309.1:c.1639A=	XP_011537611.1:p.Asn547=
NM_080722.4:c.3070A= MANE Select	NP_542453.2:p.Asn1024=
NM_139155.3:c.3079A=	NP_631894.2:p.Asn1027=
XM_011539300.2:c.2569A=	XP_011537602.1:p.Asn857=
XM_011539301.2:c.2143A=	XP_011537603.1:p.Asn715=
XM_011539302.2:c.2143A=	XP_011537604.1:p.Asn715=