Canonical Allele Identifier: CA1590863927
Gene: CAMK2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150256715C= , CM000667.2:g.150256715C= GRCh38
NC_000005.9:g.149636278C= , CM000667.1:g.149636278C= GRCh37
NC_000005.8:g.149616471C= NCBI36
NG_047040.1:g.38126G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348628.11:c.338+51G= ENSP00000261793.8:n.338+51G=
ENST00000515758.2:n.502+51G=
ENST00000672404.2:n.502+51G=
ENST00000682786.1:c.338+51G= ENSP00000507199.1:n.338+51G=
ENST00000683115.1:n.502+51G=
ENST00000683332.1:c.278+51G= ENSP00000507006.1:n.278+51G=
ENST00000683506.1:c.338+51G= ENSP00000508302.1:n.338+51G=
ENST00000684093.1:n.496+51G=
ENST00000684465.1:n.438+51G=
ENST00000398376.8:c.338+51G= ENSP00000381412.4:n.338+51G=
ENST00000510347.2:c.338+51G= ENSP00000426607.2:n.338+51G=
ENST00000671881.1:c.338+51G= MANE Select ENSP00000500386.1:n.338+51G=
ENST00000672089.1:c.338+51G= ENSP00000500700.1:n.338+51G=
ENST00000672396.1:c.338+51G= ENSP00000499987.1:n.338+51G=
ENST00000672404.1:c.183+51G=
ENST00000672479.1:c.338+51G= ENSP00000500642.1:n.338+51G=
ENST00000672752.1:c.338+51G= ENSP00000499939.1:n.338+51G=
ENST00000672785.1:c.338+51G= ENSP00000500496.1:n.338+51G=
ENST00000672829.1:c.338+51G= ENSP00000500613.1:n.338+51G=
ENST00000348628.10:c.338+51G= ENSP00000261793.8:n.338+51G=
ENST00000398376.7:c.338+51G= ENSP00000381412.3:n.338+51G=
ENST00000508662.5:n.426+51G=
ENST00000515758.1:c.-47+51G= ENSP00000427580.1:n.-47+51G=
NM_015981.3:c.338+51G= NP_057065.2:n.338+51G=
NM_171825.2:c.338+51G= NP_741960.1:n.338+51G=
NM_001363989.1:c.338+51G= NP_001350918.1:n.338+51G=
NM_001363990.1:c.338+51G= NP_001350919.1:n.338+51G=
XM_017009898.2:c.338+51G= XP_016865387.1:n.338+51G=
NM_001369025.2:c.338+51G= NP_001355954.1:n.338+51G=
NM_015981.4:c.338+51G= MANE Select NP_057065.2:n.338+51G=
NM_171825.3:c.338+51G= NP_741960.1:n.338+51G=