Canonical Allele Identifier: CA377108895

Gene: ADAMTS14

Linked Data

• MyVariant Identifiers: chr10:g.72517778A>G (hg19) ; chr10:g.70758022A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758022A>G , CM000672.2:g.70758022A>G	GRCh38
NC_000010.10:g.72517778A>G , CM000672.1:g.72517778A>G	GRCh37
NC_000010.9:g.72187784A>G	NCBI36
NG_042147.1:g.90220A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.2998A>G MANE Select	ENSP00000362303.1:p.Asn1000Asp
ENST00000373207.1:c.2998A>G	ENSP00000362303.1:p.Asn1000Asp
ENST00000373208.5:c.3007A>G	ENSP00000362304.1:p.Asn1003Asp
NM_080722.3:c.2998A>G	NP_542453.2:p.Asn1000Asp
NM_139155.2:c.3007A>G	NP_631894.2:p.Asn1003Asp
XM_011539300.1:c.2497A>G	XP_011537602.1:p.Asn833Asp
XM_011539301.1:c.2071A>G	XP_011537603.1:p.Asn691Asp
XM_011539302.1:c.2071A>G	XP_011537604.1:p.Asn691Asp
XM_011539308.1:c.*77A>G	XP_011537610.1:n.*77A>G
XM_011539309.1:c.1567A>G	XP_011537611.1:p.Asn523Asp
NM_080722.4:c.2998A>G MANE Select	NP_542453.2:p.Asn1000Asp
NM_139155.3:c.3007A>G	NP_631894.2:p.Asn1003Asp
XM_011539300.2:c.2497A>G	XP_011537602.1:p.Asn833Asp
XM_011539301.2:c.2071A>G	XP_011537603.1:p.Asn691Asp
XM_011539302.2:c.2071A>G	XP_011537604.1:p.Asn691Asp
XM_011539308.2:c.*77A>G	XP_011537610.1:n.*77A>G