Canonical Allele Identifier: CA12052750

Gene: ANKRD55

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56214829C>T , CM000667.2:g.56214829C>T	GRCh38
NC_000005.9:g.55510656C>T , CM000667.1:g.55510656C>T	GRCh37
NC_000005.8:g.55546413C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341048.9:c.58+18027G>A MANE Select	ENSP00000342295.4:n.58+18027G>A
ENST00000341048.8:c.58+18027G>A	ENSP00000342295.4:n.58+18027G>A
ENST00000504958.6:c.58+18027G>A	ENSP00000424230.1:n.58+18027G>A
ENST00000513241.2:c.-30+18412G>A	ENSP00000423507.2:n.-30+18412G>A
ENST00000519114.1:n.178+18027G>A
NM_024669.2:c.58+18027G>A	NP_078945.2:n.58+18027G>A
XM_017009852.1:c.58+18027G>A	XP_016865341.1:n.58+18027G>A
XM_017009853.1:c.58+18027G>A	XP_016865342.1:n.58+18027G>A
NM_024669.3:c.58+18027G>A MANE Select	NP_078945.2:n.58+18027G>A