Canonical Allele Identifier: CA805595420

Gene: CAMK2A

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150229830G>C , CM000667.2:g.150229830G>C	GRCh38
NC_000005.9:g.149609393G>C , CM000667.1:g.149609393G>C	GRCh37
NC_000005.8:g.149589586G>C	NCBI36
NG_047040.1:g.65011C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348628.11:c.1109+1475C>G	ENSP00000261793.8:n.1109+1475C>G
ENST00000672404.2:n.1273+1475C>G
ENST00000682786.1:c.1142+1475C>G	ENSP00000507199.1:n.1142+1475C>G
ENST00000683115.1:n.1273+1475C>G
ENST00000683332.1:c.1049+1475C>G	ENSP00000507006.1:n.1049+1475C>G
ENST00000684093.1:n.1267+1475C>G
ENST00000684431.1:n.185+1475C>G
ENST00000684465.1:n.1209+1475C>G
ENST00000398376.8:c.1034-6613C>G	ENSP00000381412.4:n.1034-6613C>G
ENST00000510347.2:c.1109+1475C>G	ENSP00000426607.2:n.1109+1475C>G
ENST00000671881.1:c.1142+1475C>G MANE Select	ENSP00000500386.1:n.1142+1475C>G
ENST00000672089.1:c.1067-1544C>G	ENSP00000500700.1:n.1067-1544C>G
ENST00000672396.1:c.1142+1475C>G	ENSP00000499987.1:n.1142+1475C>G
ENST00000672479.1:c.1109+1475C>G	ENSP00000500642.1:n.1109+1475C>G
ENST00000672752.1:c.1109+1475C>G	ENSP00000499939.1:n.1109+1475C>G
ENST00000672785.1:c.1076+1475C>G	ENSP00000500496.1:n.1076+1475C>G
ENST00000672829.1:c.1142+1475C>G	ENSP00000500613.1:n.1142+1475C>G
ENST00000348628.10:c.1109+1475C>G	ENSP00000261793.8:n.1109+1475C>G
ENST00000351010.6:n.293+1475C>G
ENST00000398376.7:c.1142+1475C>G	ENSP00000381412.3:n.1142+1475C>G
NM_015981.3:c.1142+1475C>G	NP_057065.2:n.1142+1475C>G
NM_171825.2:c.1109+1475C>G	NP_741960.1:n.1109+1475C>G
NM_001363989.1:c.1142+1475C>G	NP_001350918.1:n.1142+1475C>G
NM_001363990.1:c.1109+1475C>G	NP_001350919.1:n.1109+1475C>G
XM_017009898.2:c.1109+1475C>G	XP_016865387.1:n.1109+1475C>G
NM_001369025.2:c.1109+1475C>G	NP_001355954.1:n.1109+1475C>G
NM_015981.4:c.1142+1475C>G MANE Select	NP_057065.2:n.1142+1475C>G
NM_171825.3:c.1109+1475C>G	NP_741960.1:n.1109+1475C>G