Canonical Allele Identifier: CA377108888

Gene: ADAMTS14

Linked Data

• MyVariant Identifiers: chr10:g.72517774C>A (hg19) ; chr10:g.70758018C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758018C>A , CM000672.2:g.70758018C>A	GRCh38
NC_000010.10:g.72517774C>A , CM000672.1:g.72517774C>A	GRCh37
NC_000010.9:g.72187780C>A	NCBI36
NG_042147.1:g.90216C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.2994C>A MANE Select	ENSP00000362303.1:p.Asn998Lys
ENST00000373207.1:c.2994C>A	ENSP00000362303.1:p.Asn998Lys
ENST00000373208.5:c.3003C>A	ENSP00000362304.1:p.Asn1001Lys
NM_080722.3:c.2994C>A	NP_542453.2:p.Asn998Lys
NM_139155.2:c.3003C>A	NP_631894.2:p.Asn1001Lys
XM_011539300.1:c.2493C>A	XP_011537602.1:p.Asn831Lys
XM_011539301.1:c.2067C>A	XP_011537603.1:p.Asn689Lys
XM_011539302.1:c.2067C>A	XP_011537604.1:p.Asn689Lys
XM_011539308.1:c.*73C>A	XP_011537610.1:n.*73C>A
XM_011539309.1:c.1563C>A	XP_011537611.1:p.Asn521Lys
NM_080722.4:c.2994C>A MANE Select	NP_542453.2:p.Asn998Lys
NM_139155.3:c.3003C>A	NP_631894.2:p.Asn1001Lys
XM_011539300.2:c.2493C>A	XP_011537602.1:p.Asn831Lys
XM_011539301.2:c.2067C>A	XP_011537603.1:p.Asn689Lys
XM_011539302.2:c.2067C>A	XP_011537604.1:p.Asn689Lys
XM_011539308.2:c.*73C>A	XP_011537610.1:n.*73C>A