Canonical Allele Identifier: CA377108891

Gene: ADAMTS14

Linked Data

• MyVariant Identifiers: chr10:g.72517776C>A (hg19) ; chr10:g.70758020C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758020C>A , CM000672.2:g.70758020C>A	GRCh38
NC_000010.10:g.72517776C>A , CM000672.1:g.72517776C>A	GRCh37
NC_000010.9:g.72187782C>A	NCBI36
NG_042147.1:g.90218C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.2996C>A MANE Select	ENSP00000362303.1:p.Ala999Asp
ENST00000373207.1:c.2996C>A	ENSP00000362303.1:p.Ala999Asp
ENST00000373208.5:c.3005C>A	ENSP00000362304.1:p.Ala1002Asp
NM_080722.3:c.2996C>A	NP_542453.2:p.Ala999Asp
NM_139155.2:c.3005C>A	NP_631894.2:p.Ala1002Asp
XM_011539300.1:c.2495C>A	XP_011537602.1:p.Ala832Asp
XM_011539301.1:c.2069C>A	XP_011537603.1:p.Ala690Asp
XM_011539302.1:c.2069C>A	XP_011537604.1:p.Ala690Asp
XM_011539308.1:c.*75C>A	XP_011537610.1:n.*75C>A
XM_011539309.1:c.1565C>A	XP_011537611.1:p.Ala522Asp
NM_080722.4:c.2996C>A MANE Select	NP_542453.2:p.Ala999Asp
NM_139155.3:c.3005C>A	NP_631894.2:p.Ala1002Asp
XM_011539300.2:c.2495C>A	XP_011537602.1:p.Ala832Asp
XM_011539301.2:c.2069C>A	XP_011537603.1:p.Ala690Asp
XM_011539302.2:c.2069C>A	XP_011537604.1:p.Ala690Asp
XM_011539308.2:c.*75C>A	XP_011537610.1:n.*75C>A