Canonical Allele Identifier: CA377109062

Gene: ADAMTS14

Linked Data

• MyVariant Identifiers: chr10:g.72517936C>G (hg19) ; chr10:g.70758180C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758180C>G , CM000672.2:g.70758180C>G	GRCh38
NC_000010.10:g.72517936C>G , CM000672.1:g.72517936C>G	GRCh37
NC_000010.9:g.72187942C>G	NCBI36
NG_042147.1:g.90378C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.3073C>G MANE Select	ENSP00000362303.1:p.His1025Asp
ENST00000373207.1:c.3073C>G	ENSP00000362303.1:p.His1025Asp
ENST00000373208.5:c.3082C>G	ENSP00000362304.1:p.His1028Asp
NM_080722.3:c.3073C>G	NP_542453.2:p.His1025Asp
NM_139155.2:c.3082C>G	NP_631894.2:p.His1028Asp
XM_011539300.1:c.2572C>G	XP_011537602.1:p.His858Asp
XM_011539301.1:c.2146C>G	XP_011537603.1:p.His716Asp
XM_011539302.1:c.2146C>G	XP_011537604.1:p.His716Asp
XM_011539309.1:c.1642C>G	XP_011537611.1:p.His548Asp
NM_080722.4:c.3073C>G MANE Select	NP_542453.2:p.His1025Asp
NM_139155.3:c.3082C>G	NP_631894.2:p.His1028Asp
XM_011539300.2:c.2572C>G	XP_011537602.1:p.His858Asp
XM_011539301.2:c.2146C>G	XP_011537603.1:p.His716Asp
XM_011539302.2:c.2146C>G	XP_011537604.1:p.His716Asp