Canonical Allele Identifier: CA2675982652

Gene: CAMK2A

Linked Data

• gnomAD v4: 5-150256452-C-CAGAGAA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150256452_150256453insAGAGAA , CM000667.2:g.150256452_150256453insAGAGAA	GRCh38
NC_000005.9:g.149636015_149636016insAGAGAA , CM000667.1:g.149636015_149636016insAGAGAA	GRCh37
NC_000005.8:g.149616208_149616209insAGAGAA	NCBI36
NG_047040.1:g.38388_38389insTTCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348628.11:c.411+120_411+121insTTCTCT	ENSP00000261793.8:n.411+120_411+121insTTCTCT
ENST00000515758.2:n.575+120_575+121insTTCTCT
ENST00000672404.2:n.575+120_575+121insTTCTCT
ENST00000682786.1:c.411+120_411+121insTTCTCT	ENSP00000507199.1:n.411+120_411+121insTTCTCT
ENST00000683115.1:n.575+120_575+121insTTCTCT
ENST00000683332.1:c.351+120_351+121insTTCTCT	ENSP00000507006.1:n.351+120_351+121insTTCTCT
ENST00000683506.1:c.411+120_411+121insTTCTCT	ENSP00000508302.1:n.411+120_411+121insTTCTCT
ENST00000684093.1:n.569+120_569+121insTTCTCT
ENST00000684465.1:n.511+120_511+121insTTCTCT
ENST00000398376.8:c.411+120_411+121insTTCTCT	ENSP00000381412.4:n.411+120_411+121insTTCTCT
ENST00000510347.2:c.411+120_411+121insTTCTCT	ENSP00000426607.2:n.411+120_411+121insTTCTCT
ENST00000671881.1:c.411+120_411+121insTTCTCT MANE Select	ENSP00000500386.1:n.411+120_411+121insTTCTCT
ENST00000672089.1:c.411+120_411+121insTTCTCT	ENSP00000500700.1:n.411+120_411+121insTTCTCT
ENST00000672396.1:c.411+120_411+121insTTCTCT	ENSP00000499987.1:n.411+120_411+121insTTCTCT
ENST00000672404.1:c.256+120_256+121insTTCTCT
ENST00000672479.1:c.411+120_411+121insTTCTCT	ENSP00000500642.1:n.411+120_411+121insTTCTCT
ENST00000672752.1:c.411+120_411+121insTTCTCT	ENSP00000499939.1:n.411+120_411+121insTTCTCT
ENST00000672785.1:c.411+120_411+121insTTCTCT	ENSP00000500496.1:n.411+120_411+121insTTCTCT
ENST00000672829.1:c.411+120_411+121insTTCTCT	ENSP00000500613.1:n.411+120_411+121insTTCTCT
ENST00000348628.10:c.411+120_411+121insTTCTCT	ENSP00000261793.8:n.411+120_411+121insTTCTCT
ENST00000398376.7:c.411+120_411+121insTTCTCT	ENSP00000381412.3:n.411+120_411+121insTTCTCT
ENST00000508662.5:n.499+120_499+121insTTCTCT
ENST00000515758.1:c.27+120_27+121insTTCTCT	ENSP00000427580.1:n.27+120_27+121insTTCTCT
NM_015981.3:c.411+120_411+121insTTCTCT	NP_057065.2:n.411+120_411+121insTTCTCT
NM_171825.2:c.411+120_411+121insTTCTCT	NP_741960.1:n.411+120_411+121insTTCTCT
NM_001363989.1:c.411+120_411+121insTTCTCT	NP_001350918.1:n.411+120_411+121insTTCTCT
NM_001363990.1:c.411+120_411+121insTTCTCT	NP_001350919.1:n.411+120_411+121insTTCTCT
XM_017009898.2:c.411+120_411+121insTTCTCT	XP_016865387.1:n.411+120_411+121insTTCTCT
NM_001369025.2:c.411+120_411+121insTTCTCT	NP_001355954.1:n.411+120_411+121insTTCTCT
NM_015981.4:c.411+120_411+121insTTCTCT MANE Select	NP_057065.2:n.411+120_411+121insTTCTCT
NM_171825.3:c.411+120_411+121insTTCTCT	NP_741960.1:n.411+120_411+121insTTCTCT