Canonical Allele Identifier: CA1918399690

Gene: ADAMTS14

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758133G= , CM000672.2:g.70758133G=	GRCh38
NC_000010.10:g.72517889G= , CM000672.1:g.72517889G=	GRCh37
NC_000010.9:g.72187895G=	NCBI36
NG_042147.1:g.90331G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.3068-42G= MANE Select	ENSP00000362303.1:n.3068-42G=
ENST00000373207.1:c.3068-42G=	ENSP00000362303.1:n.3068-42G=
ENST00000373208.5:c.3077-42G=	ENSP00000362304.1:n.3077-42G=
NM_080722.3:c.3068-42G=	NP_542453.2:n.3068-42G=
NM_139155.2:c.3077-42G=	NP_631894.2:n.3077-42G=
XM_011539300.1:c.2567-42G=	XP_011537602.1:n.2567-42G=
XM_011539301.1:c.2141-42G=	XP_011537603.1:n.2141-42G=
XM_011539302.1:c.2141-42G=	XP_011537604.1:n.2141-42G=
XM_011539309.1:c.1637-42G=	XP_011537611.1:n.1637-42G=
NM_080722.4:c.3068-42G= MANE Select	NP_542453.2:n.3068-42G=
NM_139155.3:c.3077-42G=	NP_631894.2:n.3077-42G=
XM_011539300.2:c.2567-42G=	XP_011537602.1:n.2567-42G=
XM_011539301.2:c.2141-42G=	XP_011537603.1:n.2141-42G=
XM_011539302.2:c.2141-42G=	XP_011537604.1:n.2141-42G=