Canonical Allele Identifier: CA447160080

Gene: CAMK2A

Linked Data

• MyVariant Identifiers: chr5:g.149636136C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150256573C>T , CM000667.2:g.150256573C>T	GRCh38
NC_000005.9:g.149636136C>T , CM000667.1:g.149636136C>T	GRCh37
NC_000005.8:g.149616329C>T	NCBI36
NG_047040.1:g.38268G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348628.11:c.411G>A	ENSP00000261793.8:p.Lys137=
ENST00000515758.2:n.575G>A
ENST00000672404.2:n.575G>A
ENST00000682786.1:c.411G>A	ENSP00000507199.1:p.Lys137=
ENST00000683115.1:n.575G>A
ENST00000683332.1:c.351G>A	ENSP00000507006.1:p.Lys117=
ENST00000683506.1:c.411G>A	ENSP00000508302.1:p.Lys137=
ENST00000684093.1:n.569G>A
ENST00000684465.1:n.511G>A
ENST00000398376.8:c.411G>A	ENSP00000381412.4:p.Lys137=
ENST00000510347.2:c.411G>A	ENSP00000426607.2:p.Lys137=
ENST00000671881.1:c.411G>A MANE Select	ENSP00000500386.1:p.Lys137=
ENST00000672089.1:c.411G>A	ENSP00000500700.1:p.Lys137=
ENST00000672396.1:c.411G>A	ENSP00000499987.1:p.Lys137=
ENST00000672404.1:c.256G>A
ENST00000672479.1:c.411G>A	ENSP00000500642.1:p.Lys137=
ENST00000672752.1:c.411G>A	ENSP00000499939.1:p.Lys137=
ENST00000672785.1:c.411G>A	ENSP00000500496.1:p.Lys137=
ENST00000672829.1:c.411G>A	ENSP00000500613.1:p.Lys137=
ENST00000348628.10:c.411G>A	ENSP00000261793.8:p.Lys137=
ENST00000398376.7:c.411G>A	ENSP00000381412.3:p.Lys137=
ENST00000508662.5:n.499G>A
ENST00000515758.1:c.27G>A	ENSP00000427580.1:p.Lys9=
NM_015981.3:c.411G>A	NP_057065.2:p.Lys137=
NM_171825.2:c.411G>A	NP_741960.1:p.Lys137=
NM_001363989.1:c.411G>A	NP_001350918.1:p.Lys137=
NM_001363990.1:c.411G>A	NP_001350919.1:p.Lys137=
XM_017009898.2:c.411G>A	XP_016865387.1:p.Lys137=
NM_001369025.2:c.411G>A	NP_001355954.1:p.Lys137=
NM_015981.4:c.411G>A MANE Select	NP_057065.2:p.Lys137=
NM_171825.3:c.411G>A	NP_741960.1:p.Lys137=