Canonical Allele Identifier: CA1918399644

Gene: ADAMTS14

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758031G= , CM000672.2:g.70758031G=	GRCh38
NC_000010.10:g.72517787G= , CM000672.1:g.72517787G=	GRCh37
NC_000010.9:g.72187793G=	NCBI36
NG_042147.1:g.90229G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.3007G= MANE Select	ENSP00000362303.1:p.Gly1003=
ENST00000373207.1:c.3007G=	ENSP00000362303.1:p.Gly1003=
ENST00000373208.5:c.3016G=	ENSP00000362304.1:p.Gly1006=
NM_080722.3:c.3007G=	NP_542453.2:p.Gly1003=
NM_139155.2:c.3016G=	NP_631894.2:p.Gly1006=
XM_011539300.1:c.2506G=	XP_011537602.1:p.Gly836=
XM_011539301.1:c.2080G=	XP_011537603.1:p.Gly694=
XM_011539302.1:c.2080G=	XP_011537604.1:p.Gly694=
XM_011539308.1:c.*86G=	XP_011537610.1:n.*86G=
XM_011539309.1:c.1576G=	XP_011537611.1:p.Gly526=
NM_080722.4:c.3007G= MANE Select	NP_542453.2:p.Gly1003=
NM_139155.3:c.3016G=	NP_631894.2:p.Gly1006=
XM_011539300.2:c.2506G=	XP_011537602.1:p.Gly836=
XM_011539301.2:c.2080G=	XP_011537603.1:p.Gly694=
XM_011539302.2:c.2080G=	XP_011537604.1:p.Gly694=
XM_011539308.2:c.*86G=	XP_011537610.1:n.*86G=