Canonical Allele Identifier: CA1547803862

Gene: ANKRD55

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56142893G= , CM000667.2:g.56142893G=	GRCh38
NC_000005.9:g.55438720G= , CM000667.1:g.55438720G=	GRCh37
NC_000005.8:g.55474477G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341048.9:c.612+908C= MANE Select	ENSP00000342295.4:n.612+908C=
ENST00000341048.8:c.612+908C=	ENSP00000342295.4:n.612+908C=
ENST00000504958.6:c.484-15787C=	ENSP00000424230.1:n.484-15787C=
ENST00000505970.2:n.382+908C=
NM_024669.2:c.612+908C=	NP_078945.2:n.612+908C=
XM_006714691.2:c.126+908C=	XP_006714754.1:n.126+908C=
XM_011543646.1:c.-65+908C=	XP_011541948.1:n.-65+908C=
XM_017009852.1:c.612+908C=	XP_016865341.1:n.612+908C=
XM_017009853.1:c.612+908C=	XP_016865342.1:n.612+908C=
XM_017009854.1:c.126+908C=	XP_016865343.1:n.126+908C=
NM_024669.3:c.612+908C= MANE Select	NP_078945.2:n.612+908C=