Canonical Allele Identifier: CA1547803762
Gene: ANKRD55 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56142684T= , CM000667.2:g.56142684T= GRCh38
NC_000005.9:g.55438511T= , CM000667.1:g.55438511T= GRCh37
NC_000005.8:g.55474268T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000341048.9:c.612+1117A= MANE Select ENSP00000342295.4:n.612+1117A=
ENST00000341048.8:c.612+1117A= ENSP00000342295.4:n.612+1117A=
ENST00000504958.6:c.484-15578A= ENSP00000424230.1:n.484-15578A=
ENST00000505970.2:n.382+1117A=
NM_024669.2:c.612+1117A= NP_078945.2:n.612+1117A=
XM_006714691.2:c.126+1117A= XP_006714754.1:n.126+1117A=
XM_011543646.1:c.-65+1117A= XP_011541948.1:n.-65+1117A=
XM_017009852.1:c.612+1117A= XP_016865341.1:n.612+1117A=
XM_017009853.1:c.612+1117A= XP_016865342.1:n.612+1117A=
XM_017009854.1:c.126+1117A= XP_016865343.1:n.126+1117A=
NM_024669.3:c.612+1117A= MANE Select NP_078945.2:n.612+1117A=