Canonical Allele Identifier: CA368133943

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707190G>C (hg19) ; chr7:g.92077876G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077876G>C , CM000669.2:g.92077876G>C	GRCh38
NC_000007.13:g.91707190G>C , CM000669.1:g.91707190G>C	GRCh37
NC_000007.12:g.91545126G>C	NCBI36
NG_011623.1:g.142002G>C , LRG_331:g.142002G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6945+1G>C MANE Select	ENSP00000348573.3:n.6945+1G>C
ENST00000359028.7:c.7017+1G>C	ENSP00000351922.4:n.7017+1G>C
ENST00000394534.7:c.438+1G>C	ENSP00000378042.3:n.438+1G>C
ENST00000491695.2:c.1590+1G>C	ENSP00000494626.2:n.1590+1G>C
ENST00000674381.2:c.*6674+1G>C	ENSP00000501536.2:n.*6674+1G>C
ENST00000679448.1:c.6921+1G>C	ENSP00000505889.1:n.6921+1G>C
ENST00000679457.1:c.6921+1G>C	ENSP00000505450.1:n.6921+1G>C
ENST00000679474.1:n.7143+1G>C
ENST00000679521.1:c.6891+1G>C	ENSP00000505456.1:n.6891+1G>C
ENST00000679554.1:c.*6730+1G>C	ENSP00000506415.1:n.*6730+1G>C
ENST00000679722.1:n.7167+1G>C
ENST00000679821.1:c.6687+1G>C	ENSP00000506040.1:n.6687+1G>C
ENST00000680047.1:n.7143+1G>C
ENST00000680072.1:c.6768+1G>C	ENSP00000506581.1:n.6768+1G>C
ENST00000680181.1:c.6852+1G>C	ENSP00000505548.1:n.6852+1G>C
ENST00000680365.1:c.438+1G>C	ENSP00000506019.1:n.438+1G>C
ENST00000680513.1:c.6804+1G>C	ENSP00000505284.1:n.6804+1G>C
ENST00000680534.1:c.6984+1G>C	ENSP00000506674.1:n.6984+1G>C
ENST00000680766.1:c.6921+1G>C	ENSP00000505204.1:n.6921+1G>C
ENST00000680952.1:c.6921+1G>C	ENSP00000506407.1:n.6921+1G>C
ENST00000681216.1:c.438+1G>C	ENSP00000505551.1:n.438+1G>C
ENST00000681412.1:c.6945+1G>C	ENSP00000506486.1:n.6945+1G>C
ENST00000681722.1:c.6921+1G>C	ENSP00000506566.1:n.6921+1G>C
ENST00000356239.7:c.6945+1G>C	ENSP00000348573.3:n.6945+1G>C
ENST00000358100.6:c.6804+1G>C	ENSP00000350813.3:n.6804+1G>C
ENST00000359028.6:c.6978+1G>C	ENSP00000351922.3:n.6978+1G>C
ENST00000394534.6:c.483+1G>C	ENSP00000378042.2:n.483+1G>C
NM_005751.4:c.6945+1G>C , LRG_331t1:c.6945+1G>C	NP_005742.4:n.6945+1G>C
NM_147185.2:c.6921+1G>C	NP_671714.1:n.6921+1G>C
XM_006715827.1:c.6804+1G>C	XP_006715890.1:n.6804+1G>C
XM_011515709.1:c.7092+1G>C	XP_011514011.1:n.7092+1G>C
XM_011515710.1:c.7116+1G>C	XP_011514012.1:n.7116+1G>C
XM_011515711.1:c.7056+1G>C	XP_011514013.1:n.7056+1G>C
XM_011515712.1:c.7053+1G>C	XP_011514014.1:n.7053+1G>C
XM_011515713.1:c.7038+1G>C	XP_011514015.1:n.7038+1G>C
XM_011515714.1:c.7077+1G>C	XP_011514016.1:n.7077+1G>C
XM_011515716.1:c.6996+1G>C	XP_011514018.1:n.6996+1G>C
XM_011515717.1:c.6951+1G>C	XP_011514019.1:n.6951+1G>C
XM_011515718.1:c.6981+1G>C	XP_011514020.1:n.6981+1G>C
XM_011515719.1:c.6957+1G>C	XP_011514021.1:n.6957+1G>C
XM_011515720.1:c.6840+1G>C	XP_011514022.1:n.6840+1G>C
XM_011515721.1:c.1605+1G>C	XP_011514023.1:n.1605+1G>C
XM_011515722.1:c.1566+1G>C	XP_011514024.1:n.1566+1G>C
XM_017011642.2:c.7080+1G>C	XP_016867131.1:n.7080+1G>C
XM_017011643.2:c.7041+1G>C	XP_016867132.1:n.7041+1G>C
XM_017011644.2:c.7080+1G>C	XP_016867133.1:n.7080+1G>C
XM_017011645.2:c.7026+1G>C	XP_016867134.1:n.7026+1G>C
XM_017011646.2:c.7041+1G>C	XP_016867135.1:n.7041+1G>C
XM_017011647.2:c.6987+1G>C	XP_016867136.1:n.6987+1G>C
XM_017011648.2:c.6984+1G>C	XP_016867137.1:n.6984+1G>C
XM_017011649.2:c.7017+1G>C	XP_016867138.1:n.7017+1G>C
XM_017011650.2:c.6945+1G>C	XP_016867139.1:n.6945+1G>C
XM_017011651.2:c.6939+1G>C	XP_016867140.1:n.6939+1G>C
XM_017011652.2:c.7080+1G>C	XP_016867141.1:n.7080+1G>C
XM_017011653.2:c.6852+1G>C	XP_016867142.1:n.6852+1G>C
XM_017011654.2:c.6804+1G>C	XP_016867143.1:n.6804+1G>C
XM_017011655.2:c.6708+1G>C	XP_016867144.1:n.6708+1G>C
XM_017011656.2:c.6708+1G>C	XP_016867145.1:n.6708+1G>C
XM_017011657.2:c.2745+1G>C	XP_016867146.1:n.2745+1G>C
XM_017011658.2:c.1629+1G>C	XP_016867147.1:n.1629+1G>C
XM_017011659.2:c.1590+1G>C	XP_016867148.1:n.1590+1G>C
XM_017011660.2:c.1590+1G>C	XP_016867149.1:n.1590+1G>C
XM_024446631.1:c.6843+1G>C	XP_024302399.1:n.6843+1G>C
NM_147185.3:c.6921+1G>C	NP_671714.1:n.6921+1G>C
NM_001379277.1:c.1590+1G>C	NP_001366206.1:n.1590+1G>C
NM_005751.5:c.6945+1G>C MANE Select	NP_005742.4:n.6945+1G>C