Canonical Allele Identifier: CA1547803913
Gene: ANKRD55 HGNC NCBI

Linked Data

dbSNP Id: rs1757810952
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56143026G>T , CM000667.2:g.56143026G>T GRCh38
NC_000005.9:g.55438853G>T , CM000667.1:g.55438853G>T GRCh37
NC_000005.8:g.55474610G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000341048.9:c.612+775C>A MANE Select ENSP00000342295.4:n.612+775C>A
ENST00000341048.8:c.612+775C>A ENSP00000342295.4:n.612+775C>A
ENST00000504958.6:c.484-15920C>A ENSP00000424230.1:n.484-15920C>A
ENST00000505970.2:n.382+775C>A
NM_024669.2:c.612+775C>A NP_078945.2:n.612+775C>A
XM_006714691.2:c.126+775C>A XP_006714754.1:n.126+775C>A
XM_011543646.1:c.-65+775C>A XP_011541948.1:n.-65+775C>A
XM_017009852.1:c.612+775C>A XP_016865341.1:n.612+775C>A
XM_017009853.1:c.612+775C>A XP_016865342.1:n.612+775C>A
XM_017009854.1:c.126+775C>A XP_016865343.1:n.126+775C>A
NM_024669.3:c.612+775C>A MANE Select NP_078945.2:n.612+775C>A
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