Canonical Allele Identifier: CA1547792491

Gene: ANKRD55

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56119129A= , CM000667.2:g.56119129A=	GRCh38
NC_000005.9:g.55414956A= , CM000667.1:g.55414956A=	GRCh37
NC_000005.8:g.55450713A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341048.9:c.798-2347T= MANE Select	ENSP00000342295.4:n.798-2347T=
ENST00000341048.8:c.798-2347T=	ENSP00000342295.4:n.798-2347T=
ENST00000504958.6:c.669-2347T=	ENSP00000424230.1:n.669-2347T=
ENST00000505970.2:n.383-2347T=
NM_024669.2:c.798-2347T=	NP_078945.2:n.798-2347T=
XM_006714691.2:c.312-2347T=	XP_006714754.1:n.312-2347T=
XM_011543646.1:c.122-2347T=	XP_011541948.1:n.122-2347T=
XM_017009852.1:c.830-2347T=	XP_016865341.1:n.830-2347T=
XM_017009853.1:c.798-2347T=	XP_016865342.1:n.798-2347T=
XM_017009854.1:c.344-2347T=	XP_016865343.1:n.344-2347T=
NM_024669.3:c.798-2347T= MANE Select	NP_078945.2:n.798-2347T=