Canonical Allele Identifier: CA377108829

Gene: ADAMTS14

Linked Data

• MyVariant Identifiers: chr10:g.72517745C>T (hg19) ; chr10:g.70757989C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70757989C>T , CM000672.2:g.70757989C>T	GRCh38
NC_000010.10:g.72517745C>T , CM000672.1:g.72517745C>T	GRCh37
NC_000010.9:g.72187751C>T	NCBI36
NG_042147.1:g.90187C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.2965C>T MANE Select	ENSP00000362303.1:p.Gln989Ter
ENST00000373207.1:c.2965C>T	ENSP00000362303.1:p.Gln989Ter
ENST00000373208.5:c.2974C>T	ENSP00000362304.1:p.Gln992Ter
NM_080722.3:c.2965C>T	NP_542453.2:p.Gln989Ter
NM_139155.2:c.2974C>T	NP_631894.2:p.Gln992Ter
XM_011539300.1:c.2464C>T	XP_011537602.1:p.Gln822Ter
XM_011539301.1:c.2038C>T	XP_011537603.1:p.Gln680Ter
XM_011539302.1:c.2038C>T	XP_011537604.1:p.Gln680Ter
XM_011539308.1:c.*44C>T	XP_011537610.1:n.*44C>T
XM_011539309.1:c.1534C>T	XP_011537611.1:p.Gln512Ter
NM_080722.4:c.2965C>T MANE Select	NP_542453.2:p.Gln989Ter
NM_139155.3:c.2974C>T	NP_631894.2:p.Gln992Ter
XM_011539300.2:c.2464C>T	XP_011537602.1:p.Gln822Ter
XM_011539301.2:c.2038C>T	XP_011537603.1:p.Gln680Ter
XM_011539302.2:c.2038C>T	XP_011537604.1:p.Gln680Ter
XM_011539308.2:c.*44C>T	XP_011537610.1:n.*44C>T