Canonical Allele Identifier: CA368138492

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91712609A>T (hg19) ; chr7:g.92083295A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92083295A>T , CM000669.2:g.92083295A>T	GRCh38
NC_000007.13:g.91712609A>T , CM000669.1:g.91712609A>T	GRCh37
NC_000007.12:g.91550545A>T	NCBI36
NG_011623.1:g.147421A>T , LRG_331:g.147421A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.8286A>T MANE Select	ENSP00000348573.3:p.Lys2762Asn
ENST00000359028.7:c.8358A>T	ENSP00000351922.4:p.Lys2786Asn
ENST00000394534.7:c.1779A>T	ENSP00000378042.3:p.Lys593Asn
ENST00000435423.2:n.126A>T
ENST00000491695.2:c.2931A>T	ENSP00000494626.2:p.Lys977Asn
ENST00000679448.1:c.8262A>T	ENSP00000505889.1:p.Lys2754Asn
ENST00000679457.1:c.8262A>T	ENSP00000505450.1:p.Lys2754Asn
ENST00000679474.1:n.8484A>T
ENST00000679521.1:c.8232A>T	ENSP00000505456.1:p.Lys2744Asn
ENST00000679722.1:n.8508A>T
ENST00000679821.1:c.8028A>T	ENSP00000506040.1:p.Lys2676Asn
ENST00000680047.1:n.8484A>T
ENST00000680072.1:c.8109A>T	ENSP00000506581.1:p.Lys2703Asn
ENST00000680181.1:c.8193A>T	ENSP00000505548.1:p.Lys2731Asn
ENST00000680365.1:c.1779A>T	ENSP00000506019.1:p.Lys593Asn
ENST00000680513.1:c.8145A>T	ENSP00000505284.1:p.Lys2715Asn
ENST00000680534.1:c.8325A>T	ENSP00000506674.1:p.Lys2775Asn
ENST00000680766.1:c.8262A>T	ENSP00000505204.1:p.Lys2754Asn
ENST00000680952.1:c.8262A>T	ENSP00000506407.1:p.Lys2754Asn
ENST00000681216.1:c.1764+15A>T	ENSP00000505551.1:n.1764+15A>T
ENST00000681412.1:c.8286A>T	ENSP00000506486.1:p.Lys2762Asn
ENST00000681722.1:c.8262A>T	ENSP00000506566.1:p.Lys2754Asn
ENST00000356239.7:c.8286A>T	ENSP00000348573.3:p.Lys2762Asn
ENST00000358100.6:c.8145A>T	ENSP00000350813.3:p.Lys2715Asn
ENST00000359028.6:c.8319A>T	ENSP00000351922.3:p.Lys2773Asn
ENST00000394534.6:c.1824A>T	ENSP00000378042.2:p.Lys608Asn
NM_005751.4:c.8286A>T , LRG_331t1:c.8286A>T	NP_005742.4:p.Lys2762Asn
NM_147185.2:c.8262A>T	NP_671714.1:p.Lys2754Asn
XM_006715827.1:c.8145A>T	XP_006715890.1:p.Lys2715Asn
XM_011515709.1:c.8433A>T	XP_011514011.1:p.Lys2811Asn
XM_011515710.1:c.8457A>T	XP_011514012.1:p.Lys2819Asn
XM_011515711.1:c.8397A>T	XP_011514013.1:p.Lys2799Asn
XM_011515712.1:c.8394A>T	XP_011514014.1:p.Lys2798Asn
XM_011515713.1:c.8379A>T	XP_011514015.1:p.Lys2793Asn
XM_011515714.1:c.8418A>T	XP_011514016.1:p.Lys2806Asn
XM_011515716.1:c.8337A>T	XP_011514018.1:p.Lys2779Asn
XM_011515717.1:c.8292A>T	XP_011514019.1:p.Lys2764Asn
XM_011515718.1:c.8322A>T	XP_011514020.1:p.Lys2774Asn
XM_011515719.1:c.8298A>T	XP_011514021.1:p.Lys2766Asn
XM_011515720.1:c.8181A>T	XP_011514022.1:p.Lys2727Asn
XM_011515721.1:c.2946A>T	XP_011514023.1:p.Lys982Asn
XM_011515722.1:c.2907A>T	XP_011514024.1:p.Lys969Asn
XM_017011642.2:c.8421A>T	XP_016867131.1:p.Lys2807Asn
XM_017011643.2:c.8382A>T	XP_016867132.1:p.Lys2794Asn
XM_017011644.2:c.8421A>T	XP_016867133.1:p.Lys2807Asn
XM_017011645.2:c.8367A>T	XP_016867134.1:p.Lys2789Asn
XM_017011646.2:c.8382A>T	XP_016867135.1:p.Lys2794Asn
XM_017011647.2:c.8328A>T	XP_016867136.1:p.Lys2776Asn
XM_017011648.2:c.8325A>T	XP_016867137.1:p.Lys2775Asn
XM_017011649.2:c.8358A>T	XP_016867138.1:p.Lys2786Asn
XM_017011650.2:c.8286A>T	XP_016867139.1:p.Lys2762Asn
XM_017011651.2:c.8280A>T	XP_016867140.1:p.Lys2760Asn
XM_017011652.2:c.8421A>T	XP_016867141.1:p.Lys2807Asn
XM_017011653.2:c.8193A>T	XP_016867142.1:p.Lys2731Asn
XM_017011654.2:c.8145A>T	XP_016867143.1:p.Lys2715Asn
XM_017011655.2:c.8049A>T	XP_016867144.1:p.Lys2683Asn
XM_017011656.2:c.8049A>T	XP_016867145.1:p.Lys2683Asn
XM_017011657.2:c.4086A>T	XP_016867146.1:p.Lys1362Asn
XM_017011658.2:c.2970A>T	XP_016867147.1:p.Lys990Asn
XM_017011659.2:c.2931A>T	XP_016867148.1:p.Lys977Asn
XM_017011660.2:c.2931A>T	XP_016867149.1:p.Lys977Asn
XM_024446631.1:c.8184A>T	XP_024302399.1:p.Lys2728Asn
NM_147185.3:c.8262A>T	NP_671714.1:p.Lys2754Asn
NM_001379277.1:c.2931A>T	NP_001366206.1:p.Lys977Asn
NM_005751.5:c.8286A>T MANE Select	NP_005742.4:p.Lys2762Asn