Canonical Allele Identifier: CA2768887882

Gene: CAMK2A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150256456_150256457insAAACA , CM000667.2:g.150256456_150256457insAAACA	GRCh38
NC_000005.9:g.149636019_149636020insAAACA , CM000667.1:g.149636019_149636020insAAACA	GRCh37
NC_000005.8:g.149616212_149616213insAAACA	NCBI36
NG_047040.1:g.38384_38385insTGTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348628.11:c.411+116_411+117insTGTTT	ENSP00000261793.8:n.411+116_411+117insTGTTT
ENST00000515758.2:n.575+116_575+117insTGTTT
ENST00000672404.2:n.575+116_575+117insTGTTT
ENST00000682786.1:c.411+116_411+117insTGTTT	ENSP00000507199.1:n.411+116_411+117insTGTTT
ENST00000683115.1:n.575+116_575+117insTGTTT
ENST00000683332.1:c.351+116_351+117insTGTTT	ENSP00000507006.1:n.351+116_351+117insTGTTT
ENST00000683506.1:c.411+116_411+117insTGTTT	ENSP00000508302.1:n.411+116_411+117insTGTTT
ENST00000684093.1:n.569+116_569+117insTGTTT
ENST00000684465.1:n.511+116_511+117insTGTTT
ENST00000398376.8:c.411+116_411+117insTGTTT	ENSP00000381412.4:n.411+116_411+117insTGTTT
ENST00000510347.2:c.411+116_411+117insTGTTT	ENSP00000426607.2:n.411+116_411+117insTGTTT
ENST00000671881.1:c.411+116_411+117insTGTTT MANE Select	ENSP00000500386.1:n.411+116_411+117insTGTTT
ENST00000672089.1:c.411+116_411+117insTGTTT	ENSP00000500700.1:n.411+116_411+117insTGTTT
ENST00000672396.1:c.411+116_411+117insTGTTT	ENSP00000499987.1:n.411+116_411+117insTGTTT
ENST00000672404.1:c.256+116_256+117insTGTTT
ENST00000672479.1:c.411+116_411+117insTGTTT	ENSP00000500642.1:n.411+116_411+117insTGTTT
ENST00000672752.1:c.411+116_411+117insTGTTT	ENSP00000499939.1:n.411+116_411+117insTGTTT
ENST00000672785.1:c.411+116_411+117insTGTTT	ENSP00000500496.1:n.411+116_411+117insTGTTT
ENST00000672829.1:c.411+116_411+117insTGTTT	ENSP00000500613.1:n.411+116_411+117insTGTTT
ENST00000348628.10:c.411+116_411+117insTGTTT	ENSP00000261793.8:n.411+116_411+117insTGTTT
ENST00000398376.7:c.411+116_411+117insTGTTT	ENSP00000381412.3:n.411+116_411+117insTGTTT
ENST00000508662.5:n.499+116_499+117insTGTTT
ENST00000515758.1:c.27+116_27+117insTGTTT	ENSP00000427580.1:n.27+116_27+117insTGTTT
NM_015981.3:c.411+116_411+117insTGTTT	NP_057065.2:n.411+116_411+117insTGTTT
NM_171825.2:c.411+116_411+117insTGTTT	NP_741960.1:n.411+116_411+117insTGTTT
NM_001363989.1:c.411+116_411+117insTGTTT	NP_001350918.1:n.411+116_411+117insTGTTT
NM_001363990.1:c.411+116_411+117insTGTTT	NP_001350919.1:n.411+116_411+117insTGTTT
XM_017009898.2:c.411+116_411+117insTGTTT	XP_016865387.1:n.411+116_411+117insTGTTT
NM_001369025.2:c.411+116_411+117insTGTTT	NP_001355954.1:n.411+116_411+117insTGTTT
NM_015981.4:c.411+116_411+117insTGTTT MANE Select	NP_057065.2:n.411+116_411+117insTGTTT
NM_171825.3:c.411+116_411+117insTGTTT	NP_741960.1:n.411+116_411+117insTGTTT