Canonical Allele Identifier: CA7149986

Gene: AKAP6

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.32823181A>C , CM000676.2:g.32823181A>C	GRCh38
NC_000014.8:g.33292387A>C , CM000676.1:g.33292387A>C	GRCh37
NC_000014.7:g.32362138A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004274.5:c.5368A>C MANE Select	NP_004265.3:p.Thr1790Pro
ENST00000280979.9:c.5368A>C MANE Select	ENSP00000280979.4:p.Thr1790Pro
NM_004274.4:c.5368A>C	NP_004265.3:p.Thr1790Pro
ENST00000280979.8:c.5368A>C	ENSP00000280979.4:p.Thr1790Pro
ENST00000557272.1:c.3589-6667A>C	ENSP00000451247.1:n.3589-6667A>C
XM_005268219.3:c.5371A>C	XP_005268276.1:p.Thr1791Pro
XM_011537378.1:c.2656A>C	XP_011535680.1:p.Thr886Pro
XM_011537378.3:c.2656A>C	XP_011535680.1:p.Thr886Pro
XM_011537379.1:c.2587A>C	XP_011535681.1:p.Thr863Pro
XM_011537379.3:c.2587A>C	XP_011535681.1:p.Thr863Pro
XM_011537380.1:c.2587A>C	XP_011535682.1:p.Thr863Pro
XM_011537381.1:c.2437A>C	XP_011535683.1:p.Thr813Pro
XM_011537382.1:c.2437A>C	XP_011535684.1:p.Thr813Pro
XM_011537383.1:c.2353A>C	XP_011535685.1:p.Thr785Pro
XM_011537383.3:c.2353A>C	XP_011535685.1:p.Thr785Pro
XM_017021808.2:c.5371A>C	XP_016877297.1:p.Thr1791Pro
XM_017021811.2:c.2656A>C	XP_016877300.1:p.Thr886Pro
XM_024449754.1:c.5371A>C	XP_024305522.1:p.Thr1791Pro
XM_024449755.1:c.5371A>C	XP_024305523.1:p.Thr1791Pro
XM_024449756.1:c.5371A>C	XP_024305524.1:p.Thr1791Pro
XM_024449757.1:c.5371A>C	XP_024305525.1:p.Thr1791Pro