Canonical Allele Identifier: CA1918399638

Gene: ADAMTS14

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758018C= , CM000672.2:g.70758018C=	GRCh38
NC_000010.10:g.72517774C= , CM000672.1:g.72517774C=	GRCh37
NC_000010.9:g.72187780C=	NCBI36
NG_042147.1:g.90216C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.2994C= MANE Select	ENSP00000362303.1:p.Asn998=
ENST00000373207.1:c.2994C=	ENSP00000362303.1:p.Asn998=
ENST00000373208.5:c.3003C=	ENSP00000362304.1:p.Asn1001=
NM_080722.3:c.2994C=	NP_542453.2:p.Asn998=
NM_139155.2:c.3003C=	NP_631894.2:p.Asn1001=
XM_011539300.1:c.2493C=	XP_011537602.1:p.Asn831=
XM_011539301.1:c.2067C=	XP_011537603.1:p.Asn689=
XM_011539302.1:c.2067C=	XP_011537604.1:p.Asn689=
XM_011539308.1:c.*73C=	XP_011537610.1:n.*73C=
XM_011539309.1:c.1563C=	XP_011537611.1:p.Asn521=
NM_080722.4:c.2994C= MANE Select	NP_542453.2:p.Asn998=
NM_139155.3:c.3003C=	NP_631894.2:p.Asn1001=
XM_011539300.2:c.2493C=	XP_011537602.1:p.Asn831=
XM_011539301.2:c.2067C=	XP_011537603.1:p.Asn689=
XM_011539302.2:c.2067C=	XP_011537604.1:p.Asn689=
XM_011539308.2:c.*73C=	XP_011537610.1:n.*73C=