Canonical Allele Identifier: CA1918391615

Gene: ADAMTS14

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70740834C= , CM000672.2:g.70740834C=	GRCh38
NC_000010.10:g.72500590C= , CM000672.1:g.72500590C=	GRCh37
NC_000010.9:g.72170596C=	NCBI36
NG_042147.1:g.73032C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000373207.2:c.1749-153C= MANE Select	ENSP00000362303.1:n.1749-153C=
ENST00000373207.1:c.1749-153C=	ENSP00000362303.1:n.1749-153C=
ENST00000373208.5:c.1758-153C=	ENSP00000362304.1:n.1758-153C=
NM_080722.3:c.1749-153C=	NP_542453.2:n.1749-153C=
NM_139155.2:c.1758-153C=	NP_631894.2:n.1758-153C=
XM_011539300.1:c.1758-153C=	XP_011537602.1:n.1758-153C=
XM_011539301.1:c.822-153C=	XP_011537603.1:n.822-153C=
XM_011539302.1:c.822-153C=	XP_011537604.1:n.822-153C=
XM_011539303.1:c.1758-153C=	XP_011537605.1:n.1758-153C=
XM_011539304.1:c.1758-153C=	XP_011537606.1:n.1758-153C=
XM_011539305.1:c.1758-153C=	XP_011537607.1:n.1758-153C=
XM_011539306.1:c.1758-153C=	XP_011537608.1:n.1758-153C=
XM_011539307.1:c.1758-153C=	XP_011537609.1:n.1758-153C=
XM_011539308.1:c.1758-153C=	XP_011537610.1:n.1758-153C=
XM_011539309.1:c.318-153C=	XP_011537611.1:n.318-153C=
NM_080722.4:c.1749-153C= MANE Select	NP_542453.2:n.1749-153C=
NM_139155.3:c.1758-153C=	NP_631894.2:n.1758-153C=
XM_011539300.2:c.1758-153C=	XP_011537602.1:n.1758-153C=
XM_011539301.2:c.822-153C=	XP_011537603.1:n.822-153C=
XM_011539302.2:c.822-153C=	XP_011537604.1:n.822-153C=
XM_011539303.2:c.1758-153C=	XP_011537605.1:n.1758-153C=
XM_011539306.2:c.1758-153C=	XP_011537608.1:n.1758-153C=
XM_011539307.2:c.1758-153C=	XP_011537609.1:n.1758-153C=
XM_011539308.2:c.1758-153C=	XP_011537610.1:n.1758-153C=
XR_001747025.1:n.2043-153C=