Canonical Allele Identifier: CA576705553

Gene: AKAP9

Linked Data

• gnomAD v2: 7-91669977-TACTA-T
• gnomAD v4: 7-92040663-TACTA-T
• MyVariant Identifiers: chr7:g.91669978_91669981del (hg19) ; chr7:g.92040664_92040667del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92040664_92040667del , CM000669.2:g.92040664_92040667del	GRCh38
NC_000007.13:g.91669978_91669981del , CM000669.1:g.91669978_91669981del	GRCh37
NC_000007.12:g.91507914_91507917del	NCBI36
NG_011623.1:g.104790_104793del , LRG_331:g.104790_104793del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.4693-10_4693-7del MANE Select	ENSP00000348573.3:n.4693-10_4693-7del
ENST00000359028.7:c.4693-10_4693-7del	ENSP00000351922.4:n.4693-10_4693-7del
ENST00000674381.2:c.*4422-10_*4422-7del	ENSP00000501536.2:n.*4422-10_*4422-7del
ENST00000679448.1:c.4693-10_4693-7del	ENSP00000505889.1:n.4693-10_4693-7del
ENST00000679457.1:c.4693-10_4693-7del	ENSP00000505450.1:n.4693-10_4693-7del
ENST00000679474.1:n.4915-10_4915-7del
ENST00000679521.1:c.4639-10_4639-7del	ENSP00000505456.1:n.4639-10_4639-7del
ENST00000679554.1:c.*4478-10_*4478-7del	ENSP00000506415.1:n.*4478-10_*4478-7del
ENST00000679722.1:n.4915-10_4915-7del
ENST00000679821.1:c.4435-10_4435-7del	ENSP00000506040.1:n.4435-10_4435-7del
ENST00000680047.1:n.4915-10_4915-7del
ENST00000680072.1:c.4693-10_4693-7del	ENSP00000506581.1:n.4693-10_4693-7del
ENST00000680074.1:n.4915-10_4915-7del
ENST00000680181.1:c.4600-10_4600-7del	ENSP00000505548.1:n.4600-10_4600-7del
ENST00000680513.1:c.4693-10_4693-7del	ENSP00000505284.1:n.4693-10_4693-7del
ENST00000680534.1:c.4693-10_4693-7del	ENSP00000506674.1:n.4693-10_4693-7del
ENST00000680766.1:c.4693-10_4693-7del	ENSP00000505204.1:n.4693-10_4693-7del
ENST00000680952.1:c.4693-10_4693-7del	ENSP00000506407.1:n.4693-10_4693-7del
ENST00000681412.1:c.4693-10_4693-7del	ENSP00000506486.1:n.4693-10_4693-7del
ENST00000681722.1:c.4693-10_4693-7del	ENSP00000506566.1:n.4693-10_4693-7del
ENST00000356239.7:c.4693-10_4693-7del	ENSP00000348573.3:n.4693-10_4693-7del
ENST00000358100.6:c.4693-10_4693-7del	ENSP00000350813.3:n.4693-10_4693-7del
ENST00000359028.6:c.4726-10_4726-7del	ENSP00000351922.3:n.4726-10_4726-7del
ENST00000493453.1:n.4913-10_4913-7del
ENST00000619023.4:c.4717-10_4717-7del	ENSP00000480807.1:n.4717-10_4717-7del
NM_005751.4:c.4693-10_4693-7del , LRG_331t1:c.4693-10_4693-7del	NP_005742.4:n.4693-10_4693-7del
NM_147185.2:c.4693-10_4693-7del	NP_671714.1:n.4693-10_4693-7del
XM_006715827.1:c.4693-10_4693-7del	XP_006715890.1:n.4693-10_4693-7del
XM_011515709.1:c.4729-10_4729-7del	XP_011514011.1:n.4729-10_4729-7del
XM_011515710.1:c.4729-10_4729-7del	XP_011514012.1:n.4729-10_4729-7del
XM_011515711.1:c.4693-10_4693-7del	XP_011514013.1:n.4693-10_4693-7del
XM_011515712.1:c.4729-10_4729-7del	XP_011514014.1:n.4729-10_4729-7del
XM_011515713.1:c.4675-10_4675-7del	XP_011514015.1:n.4675-10_4675-7del
XM_011515714.1:c.4729-10_4729-7del	XP_011514016.1:n.4729-10_4729-7del
XM_011515716.1:c.4729-10_4729-7del	XP_011514018.1:n.4729-10_4729-7del
XM_011515717.1:c.4729-10_4729-7del	XP_011514019.1:n.4729-10_4729-7del
XM_011515718.1:c.4729-10_4729-7del	XP_011514020.1:n.4729-10_4729-7del
XM_011515719.1:c.4729-10_4729-7del	XP_011514021.1:n.4729-10_4729-7del
XM_011515720.1:c.4729-10_4729-7del	XP_011514022.1:n.4729-10_4729-7del
XM_017011642.2:c.4693-10_4693-7del	XP_016867131.1:n.4693-10_4693-7del
XM_017011643.2:c.4693-10_4693-7del	XP_016867132.1:n.4693-10_4693-7del
XM_017011644.2:c.4693-10_4693-7del	XP_016867133.1:n.4693-10_4693-7del
XM_017011645.2:c.4639-10_4639-7del	XP_016867134.1:n.4639-10_4639-7del
XM_017011646.2:c.4693-10_4693-7del	XP_016867135.1:n.4693-10_4693-7del
XM_017011647.2:c.4600-10_4600-7del	XP_016867136.1:n.4600-10_4600-7del
XM_017011648.2:c.4693-10_4693-7del	XP_016867137.1:n.4693-10_4693-7del
XM_017011649.2:c.4693-10_4693-7del	XP_016867138.1:n.4693-10_4693-7del
XM_017011650.2:c.4693-10_4693-7del	XP_016867139.1:n.4693-10_4693-7del
XM_017011651.2:c.4693-10_4693-7del	XP_016867140.1:n.4693-10_4693-7del
XM_017011652.2:c.4693-10_4693-7del	XP_016867141.1:n.4693-10_4693-7del
XM_017011653.2:c.4600-10_4600-7del	XP_016867142.1:n.4600-10_4600-7del
XM_017011654.2:c.4693-10_4693-7del	XP_016867143.1:n.4693-10_4693-7del
XM_017011655.2:c.4321-10_4321-7del	XP_016867144.1:n.4321-10_4321-7del
XM_017011656.2:c.4321-10_4321-7del	XP_016867145.1:n.4321-10_4321-7del
XM_017011657.2:c.358-10_358-7del	XP_016867146.1:n.358-10_358-7del
XM_024446631.1:c.4693-10_4693-7del	XP_024302399.1:n.4693-10_4693-7del
NM_147185.3:c.4693-10_4693-7del	NP_671714.1:n.4693-10_4693-7del
NM_005751.5:c.4693-10_4693-7del MANE Select	NP_005742.4:n.4693-10_4693-7del