Canonical Allele Identifier: CA15410896
Gene: ANKRD55 HGNC NCBI

Linked Data

dbSNP Id: rs10065637

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56143024C>T , CM000667.2:g.56143024C>T GRCh38
NC_000005.9:g.55438851C>T , CM000667.1:g.55438851C>T GRCh37
NC_000005.8:g.55474608C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000341048.9:c.612+777G>A MANE Select ENSP00000342295.4:p.=
ENST00000341048.8:c.612+777G>A ENSP00000342295.4:p.=
ENST00000504958.6:c.484-15918G>A ENSP00000424230.1:p.=
ENST00000505970.2:n.382+777G>A
NM_024669.2:c.612+777G>A NP_078945.2:p.=
XM_006714691.2:c.126+777G>A XP_006714754.1:p.=
XM_011543646.1:c.-65+777G>A XP_011541948.1:p.=
XM_017009852.1:c.612+777G>A XP_016865341.1:p.=
XM_017009853.1:c.612+777G>A XP_016865342.1:p.=
XM_017009854.1:c.126+777G>A XP_016865343.1:p.=
NM_024669.3:c.612+777G>A MANE Select NP_078945.2:p.=