Canonical Allele Identifier: CA148344011

Gene: AKAP7

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131149096C>A , CM000668.2:g.131149096C>A	GRCh38
NC_000006.11:g.131470236C>A , CM000668.1:g.131470236C>A	GRCh37
NC_000006.10:g.131511929C>A	NCBI36
NG_029123.1:g.18411C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683794.1:c.151+3680C>A	ENSP00000506952.1:n.151+3680C>A
ENST00000431975.7:c.151+3680C>A MANE Select	ENSP00000405252.2:n.151+3680C>A
ENST00000366358.2:n.506+3680C>A
ENST00000431975.6:c.151+3680C>A	ENSP00000405252.2:n.151+3680C>A
ENST00000541650.5:c.148+3680C>A	ENSP00000441048.1:n.148+3680C>A
NM_016377.3:c.151+3680C>A	NP_057461.2:n.151+3680C>A
XM_005267228.1:c.151+3680C>A	XP_005267285.1:n.151+3680C>A
XM_005267229.3:c.85+3680C>A	XP_005267286.1:n.85+3680C>A
XM_006715614.2:c.151+3680C>A	XP_006715677.1:n.151+3680C>A
XM_011536262.1:c.151+3680C>A	XP_011534564.1:n.151+3680C>A
XR_427979.1:n.184+3680C>A
XR_942636.1:n.184+3680C>A
XM_005267229.4:c.85+3680C>A	XP_005267286.1:n.85+3680C>A
XM_017011506.1:c.151+3680C>A	XP_016866995.1:n.151+3680C>A
XM_017011507.1:c.151+3680C>A	XP_016866996.1:n.151+3680C>A
XM_017011508.1:c.181+3680C>A	XP_016866997.1:n.181+3680C>A
XM_017011509.1:c.163+3680C>A	XP_016866998.1:n.163+3680C>A
XM_024446589.1:c.151+3680C>A	XP_024302357.1:n.151+3680C>A
XR_001743754.2:n.184+3680C>A
XR_001743755.2:n.184+3680C>A
XR_002956317.1:n.184+3680C>A
XR_002956318.1:n.184+3680C>A
XR_942636.2:n.184+3680C>A
NM_016377.4:c.151+3680C>A MANE Select	NP_057461.2:n.151+3680C>A
NM_001376570.1:c.151+3680C>A	NP_001363499.1:n.151+3680C>A
NR_164832.1:n.1047+3680C>A
NR_164833.1:n.1112+3680C>A
NR_164834.1:n.448+3680C>A
NM_001387860.1:c.20-10963C>A	NP_001374789.1:n.20-10963C>A
NM_001387861.1:c.151+3680C>A	NP_001374790.1:n.151+3680C>A
NM_001387862.1:c.151+3680C>A	NP_001374791.1:n.151+3680C>A
NM_001387863.1:c.85+3680C>A	NP_001374792.1:n.85+3680C>A
NR_170716.1:n.448+3680C>A
NR_170717.1:n.448+3680C>A