Canonical Allele Identifier: CA2566954257
Gene: ANKRD55 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56142884G>T , CM000667.2:g.56142884G>T GRCh38
NC_000005.9:g.55438711G>T , CM000667.1:g.55438711G>T GRCh37
NC_000005.8:g.55474468G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000341048.9:c.612+917C>A MANE Select ENSP00000342295.4:n.612+917C>A
ENST00000341048.8:c.612+917C>A ENSP00000342295.4:n.612+917C>A
ENST00000504958.6:c.484-15778C>A ENSP00000424230.1:n.484-15778C>A
ENST00000505970.2:n.382+917C>A
NM_024669.2:c.612+917C>A NP_078945.2:n.612+917C>A
XM_006714691.2:c.126+917C>A XP_006714754.1:n.126+917C>A
XM_011543646.1:c.-65+917C>A XP_011541948.1:n.-65+917C>A
XM_017009852.1:c.612+917C>A XP_016865341.1:n.612+917C>A
XM_017009853.1:c.612+917C>A XP_016865342.1:n.612+917C>A
XM_017009854.1:c.126+917C>A XP_016865343.1:n.126+917C>A
NM_024669.3:c.612+917C>A MANE Select NP_078945.2:n.612+917C>A
Search 100 bp 5'
Search 100 bp 3'