Canonical Allele Identifier: CA1918399563
Gene: ADAMTS14 HGNC NCBI

Linked Data

dbSNP Id: rs1842514994

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70757897del , CM000672.2:g.70757897del GRCh38
NC_000010.10:g.72517653del , CM000672.1:g.72517653del GRCh37
NC_000010.9:g.72187659del NCBI36
NG_042147.1:g.90095del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373207.2:c.2938-65del MANE Select ENSP00000362303.1:n.2938-65del
ENST00000373207.1:c.2938-65del ENSP00000362303.1:n.2938-65del
ENST00000373208.5:c.2947-65del ENSP00000362304.1:n.2947-65del
NM_080722.3:c.2938-65del NP_542453.2:n.2938-65del
NM_139155.2:c.2947-65del NP_631894.2:n.2947-65del
XM_011539300.1:c.2437-65del XP_011537602.1:n.2437-65del
XM_011539301.1:c.2011-65del XP_011537603.1:n.2011-65del
XM_011539302.1:c.2011-65del XP_011537604.1:n.2011-65del
XM_011539308.1:c.*17-65del XP_011537610.1:n.*17-65del
XM_011539309.1:c.1507-65del XP_011537611.1:n.1507-65del
NM_080722.4:c.2938-65del MANE Select NP_542453.2:n.2938-65del
NM_139155.3:c.2947-65del NP_631894.2:n.2947-65del
XM_011539300.2:c.2437-65del XP_011537602.1:n.2437-65del
XM_011539301.2:c.2011-65del XP_011537603.1:n.2011-65del
XM_011539302.2:c.2011-65del XP_011537604.1:n.2011-65del
XM_011539308.2:c.*17-65del XP_011537610.1:n.*17-65del