Canonical Allele Identifier: CA1918399573
Gene: ADAMTS14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70757916A= , CM000672.2:g.70757916A= GRCh38
NC_000010.10:g.72517672A= , CM000672.1:g.72517672A= GRCh37
NC_000010.9:g.72187678A= NCBI36
NG_042147.1:g.90114A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373207.2:c.2938-46A= MANE Select ENSP00000362303.1:n.2938-46A=
ENST00000373207.1:c.2938-46A= ENSP00000362303.1:n.2938-46A=
ENST00000373208.5:c.2947-46A= ENSP00000362304.1:n.2947-46A=
NM_080722.3:c.2938-46A= NP_542453.2:n.2938-46A=
NM_139155.2:c.2947-46A= NP_631894.2:n.2947-46A=
XM_011539300.1:c.2437-46A= XP_011537602.1:n.2437-46A=
XM_011539301.1:c.2011-46A= XP_011537603.1:n.2011-46A=
XM_011539302.1:c.2011-46A= XP_011537604.1:n.2011-46A=
XM_011539308.1:c.*17-46A= XP_011537610.1:n.*17-46A=
XM_011539309.1:c.1507-46A= XP_011537611.1:n.1507-46A=
NM_080722.4:c.2938-46A= MANE Select NP_542453.2:n.2938-46A=
NM_139155.3:c.2947-46A= NP_631894.2:n.2947-46A=
XM_011539300.2:c.2437-46A= XP_011537602.1:n.2437-46A=
XM_011539301.2:c.2011-46A= XP_011537603.1:n.2011-46A=
XM_011539302.2:c.2011-46A= XP_011537604.1:n.2011-46A=
XM_011539308.2:c.*17-46A= XP_011537610.1:n.*17-46A=