Canonical Allele Identifier: CA1547803853

Gene: ANKRD55

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56142884G= , CM000667.2:g.56142884G=	GRCh38
NC_000005.9:g.55438711G= , CM000667.1:g.55438711G=	GRCh37
NC_000005.8:g.55474468G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000341048.9:c.612+917C= MANE Select	ENSP00000342295.4:n.612+917C=
ENST00000341048.8:c.612+917C=	ENSP00000342295.4:n.612+917C=
ENST00000504958.6:c.484-15778C=	ENSP00000424230.1:n.484-15778C=
ENST00000505970.2:n.382+917C=
NM_024669.2:c.612+917C=	NP_078945.2:n.612+917C=
XM_006714691.2:c.126+917C=	XP_006714754.1:n.126+917C=
XM_011543646.1:c.-65+917C=	XP_011541948.1:n.-65+917C=
XM_017009852.1:c.612+917C=	XP_016865341.1:n.612+917C=
XM_017009853.1:c.612+917C=	XP_016865342.1:n.612+917C=
XM_017009854.1:c.126+917C=	XP_016865343.1:n.126+917C=
NM_024669.3:c.612+917C= MANE Select	NP_078945.2:n.612+917C=