Canonical Allele Identifier: CA1547836477

Gene: ANKRD55

Genomic Alleles

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

Transcript Alleles

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