Canonical Allele Identifier: CA2127859658

Gene: AKAP6

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.32813264C= , CM000676.2:g.32813264C=	GRCh38
NC_000014.8:g.33282470C= , CM000676.1:g.33282470C=	GRCh37
NC_000014.7:g.32352221C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280979.9:c.3589-8138C= MANE Select	ENSP00000280979.4:n.3589-8138C=
ENST00000280979.8:c.3589-8138C=	ENSP00000280979.4:n.3589-8138C=
ENST00000557272.1:c.3589-16584C=	ENSP00000451247.1:n.3589-16584C=
NM_004274.4:c.3589-8138C=	NP_004265.3:n.3589-8138C=
XM_005268219.3:c.3592-8138C=	XP_005268276.1:n.3592-8138C=
XM_011537378.1:c.877-8138C=	XP_011535680.1:n.877-8138C=
XM_011537379.1:c.808-8138C=	XP_011535681.1:n.808-8138C=
XM_011537380.1:c.808-8138C=	XP_011535682.1:n.808-8138C=
XM_011537381.1:c.658-8138C=	XP_011535683.1:n.658-8138C=
XM_011537382.1:c.658-8138C=	XP_011535684.1:n.658-8138C=
XM_011537383.1:c.574-8138C=	XP_011535685.1:n.574-8138C=
XM_011537378.3:c.877-8138C=	XP_011535680.1:n.877-8138C=
XM_011537379.3:c.808-8138C=	XP_011535681.1:n.808-8138C=
XM_011537383.3:c.574-8138C=	XP_011535685.1:n.574-8138C=
XM_017021808.2:c.3592-8138C=	XP_016877297.1:n.3592-8138C=
XM_017021811.2:c.877-8138C=	XP_016877300.1:n.877-8138C=
XM_024449754.1:c.3592-8138C=	XP_024305522.1:n.3592-8138C=
XM_024449755.1:c.3592-8138C=	XP_024305523.1:n.3592-8138C=
XM_024449756.1:c.3592-8138C=	XP_024305524.1:n.3592-8138C=
XM_024449757.1:c.3592-8138C=	XP_024305525.1:n.3592-8138C=
NM_004274.5:c.3589-8138C= MANE Select	NP_004265.3:n.3589-8138C=