Canonical Allele Identifier: CA1918399666

Gene: ADAMTS14

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758081C= , CM000672.2:g.70758081C=	GRCh38
NC_000010.10:g.72517837C= , CM000672.1:g.72517837C=	GRCh37
NC_000010.9:g.72187843C=	NCBI36
NG_042147.1:g.90279C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000373207.2:c.3057C= MANE Select	ENSP00000362303.1:p.Pro1019=
ENST00000373207.1:c.3057C=	ENSP00000362303.1:p.Pro1019=
ENST00000373208.5:c.3066C=	ENSP00000362304.1:p.Pro1022=
NM_080722.3:c.3057C=	NP_542453.2:p.Pro1019=
NM_139155.2:c.3066C=	NP_631894.2:p.Pro1022=
XM_011539300.1:c.2556C=	XP_011537602.1:p.Pro852=
XM_011539301.1:c.2130C=	XP_011537603.1:p.Pro710=
XM_011539302.1:c.2130C=	XP_011537604.1:p.Pro710=
XM_011539309.1:c.1626C=	XP_011537611.1:p.Pro542=
NM_080722.4:c.3057C= MANE Select	NP_542453.2:p.Pro1019=
NM_139155.3:c.3066C=	NP_631894.2:p.Pro1022=
XM_011539300.2:c.2556C=	XP_011537602.1:p.Pro852=
XM_011539301.2:c.2130C=	XP_011537603.1:p.Pro710=
XM_011539302.2:c.2130C=	XP_011537604.1:p.Pro710=