Canonical Allele Identifier: CA377109012

Gene: ADAMTS14

Linked Data

• MyVariant Identifiers: chr10:g.72517833T>G (hg19) ; chr10:g.70758077T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758077T>G , CM000672.2:g.70758077T>G	GRCh38
NC_000010.10:g.72517833T>G , CM000672.1:g.72517833T>G	GRCh37
NC_000010.9:g.72187839T>G	NCBI36
NG_042147.1:g.90275T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.3053T>G MANE Select	ENSP00000362303.1:p.Leu1018Arg
ENST00000373207.1:c.3053T>G	ENSP00000362303.1:p.Leu1018Arg
ENST00000373208.5:c.3062T>G	ENSP00000362304.1:p.Leu1021Arg
NM_080722.3:c.3053T>G	NP_542453.2:p.Leu1018Arg
NM_139155.2:c.3062T>G	NP_631894.2:p.Leu1021Arg
XM_011539300.1:c.2552T>G	XP_011537602.1:p.Leu851Arg
XM_011539301.1:c.2126T>G	XP_011537603.1:p.Leu709Arg
XM_011539302.1:c.2126T>G	XP_011537604.1:p.Leu709Arg
XM_011539309.1:c.1622T>G	XP_011537611.1:p.Leu541Arg
NM_080722.4:c.3053T>G MANE Select	NP_542453.2:p.Leu1018Arg
NM_139155.3:c.3062T>G	NP_631894.2:p.Leu1021Arg
XM_011539300.2:c.2552T>G	XP_011537602.1:p.Leu851Arg
XM_011539301.2:c.2126T>G	XP_011537603.1:p.Leu709Arg
XM_011539302.2:c.2126T>G	XP_011537604.1:p.Leu709Arg