Canonical Allele Identifier: CA1547803881

Gene: ANKRD55

Linked Data

• dbSNP Id: rs1757808484

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56142955A>G , CM000667.2:g.56142955A>G	GRCh38
NC_000005.9:g.55438782A>G , CM000667.1:g.55438782A>G	GRCh37
NC_000005.8:g.55474539A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000341048.9:c.612+846T>C MANE Select	ENSP00000342295.4:n.612+846T>C
ENST00000341048.8:c.612+846T>C	ENSP00000342295.4:n.612+846T>C
ENST00000504958.6:c.484-15849T>C	ENSP00000424230.1:n.484-15849T>C
ENST00000505970.2:n.382+846T>C
NM_024669.2:c.612+846T>C	NP_078945.2:n.612+846T>C
XM_006714691.2:c.126+846T>C	XP_006714754.1:n.126+846T>C
XM_011543646.1:c.-65+846T>C	XP_011541948.1:n.-65+846T>C
XM_017009852.1:c.612+846T>C	XP_016865341.1:n.612+846T>C
XM_017009853.1:c.612+846T>C	XP_016865342.1:n.612+846T>C
XM_017009854.1:c.126+846T>C	XP_016865343.1:n.126+846T>C
NM_024669.3:c.612+846T>C MANE Select	NP_078945.2:n.612+846T>C