Canonical Allele Identifier: CA1547806387

Gene: ANKRD55

Linked Data

• dbSNP Id: rs7731626

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56148856G>C , CM000667.2:g.56148856G>C	GRCh38
NC_000005.9:g.55444683G>C , CM000667.1:g.55444683G>C	GRCh37
NC_000005.8:g.55480440G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000341048.9:c.484-4927C>G MANE Select	ENSP00000342295.4:n.484-4927C>G
ENST00000341048.8:c.484-4927C>G	ENSP00000342295.4:n.484-4927C>G
ENST00000504958.6:c.483+10977C>G	ENSP00000424230.1:n.483+10977C>G
ENST00000505970.2:n.254-4927C>G
ENST00000513241.2:c.397-4927C>G	ENSP00000423507.2:n.397-4927C>G
NM_024669.2:c.484-4927C>G	NP_078945.2:n.484-4927C>G
XM_006714691.2:c.-3-4927C>G	XP_006714754.1:n.-3-4927C>G
XM_017009852.1:c.484-4927C>G	XP_016865341.1:n.484-4927C>G
XM_017009853.1:c.484-4927C>G	XP_016865342.1:n.484-4927C>G
XM_017009854.1:c.-3-4927C>G	XP_016865343.1:n.-3-4927C>G
NM_024669.3:c.484-4927C>G MANE Select	NP_078945.2:n.484-4927C>G