Canonical Allele Identifier: CA1918399626

Gene: ADAMTS14

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70757995_70757996delinsCG , CM000672.2:g.70757995_70757996delinsCG	GRCh38
NC_000010.10:g.72517751_72517752delinsCG , CM000672.1:g.72517751_72517752delinsCG	GRCh37
NC_000010.9:g.72187757_72187758delinsCG	NCBI36
NG_042147.1:g.90193_90194delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.2971_2972delinsCG MANE Select	ENSP00000362303.1:p.Arg991=
ENST00000373207.1:c.2971_2972delinsCG	ENSP00000362303.1:p.Arg991=
ENST00000373208.5:c.2980_2981delinsCG	ENSP00000362304.1:p.Arg994=
NM_080722.3:c.2971_2972delinsCG	NP_542453.2:p.Arg991=
NM_139155.2:c.2980_2981delinsCG	NP_631894.2:p.Arg994=
XM_011539300.1:c.2470_2471delinsCG	XP_011537602.1:p.Arg824=
XM_011539301.1:c.2044_2045delinsCG	XP_011537603.1:p.Arg682=
XM_011539302.1:c.2044_2045delinsCG	XP_011537604.1:p.Arg682=
XM_011539308.1:c.*50_*51delinsCG	XP_011537610.1:n.*50_*51delinsCG
XM_011539309.1:c.1540_1541delinsCG	XP_011537611.1:p.Arg514=
NM_080722.4:c.2971_2972delinsCG MANE Select	NP_542453.2:p.Arg991=
NM_139155.3:c.2980_2981delinsCG	NP_631894.2:p.Arg994=
XM_011539300.2:c.2470_2471delinsCG	XP_011537602.1:p.Arg824=
XM_011539301.2:c.2044_2045delinsCG	XP_011537603.1:p.Arg682=
XM_011539302.2:c.2044_2045delinsCG	XP_011537604.1:p.Arg682=
XM_011539308.2:c.*50_*51delinsCG	XP_011537610.1:n.*50_*51delinsCG