Canonical Allele Identifier: CA1703668355
Gene: CAMK2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44220272C= , CM000669.2:g.44220272C= GRCh38
NC_000007.13:g.44259871C= , CM000669.1:g.44259871C= GRCh37
NC_000007.12:g.44226396C= NCBI36
NG_029407.1:g.110360G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433930.2:c.818G=
ENST00000470984.6:c.1032G= ENSP00000514879.1:p.Pro344=
ENST00000484972.6:n.1492G=
ENST00000700233.1:c.1341G= ENSP00000514871.1:p.Pro447=
ENST00000700234.1:c.402G=
ENST00000700235.1:c.1476G= ENSP00000514874.1:p.Pro492=
ENST00000700236.1:c.792G=
ENST00000700237.1:c.1032G= ENSP00000514876.1:p.Pro344=
ENST00000700238.1:c.960G= ENSP00000514877.1:p.Pro320=
ENST00000700239.1:c.1288G=
ENST00000700240.1:c.987G= ENSP00000514880.1:p.Pro329=
ENST00000700241.1:c.1421G=
ENST00000700283.1:c.1301G=
ENST00000700284.1:c.*1648G= ENSP00000514917.1:n.*1648G=
ENST00000700285.1:c.1419G= ENSP00000514918.1:p.Pro473=
ENST00000700286.1:n.1920G=
ENST00000700287.1:c.1432G=
ENST00000700288.1:c.954G= ENSP00000514920.1:p.Pro318=
ENST00000700289.1:n.1164G=
ENST00000700290.1:c.957G= ENSP00000514921.1:p.Pro319=
ENST00000700291.1:c.1216G= ENSP00000514922.1:p.Asp406=
ENST00000395749.7:c.1791G= MANE Select ENSP00000379098.2:p.Pro597=
ENST00000258682.10:c.1344G= ENSP00000258682.6:p.Pro448=
ENST00000346990.8:c.1140G= ENSP00000326518.5:p.Pro380=
ENST00000347193.8:c.1269G= ENSP00000326544.6:p.Pro423=
ENST00000350811.7:c.1419G= ENSP00000326375.5:p.Pro473=
ENST00000353185.7:c.*212G= ENSP00000326600.4:n.*212G=
ENST00000353625.8:c.1230G= ENSP00000326427.5:p.Pro410=
ENST00000358707.7:c.1302G= ENSP00000351542.3:p.Pro434=
ENST00000395747.6:c.1347G= ENSP00000379096.2:p.Pro449=
ENST00000395749.6:c.1791G= ENSP00000379098.2:p.Pro597=
ENST00000425809.5:c.345G= ENSP00000410445.1:p.Pro115=
ENST00000440254.6:c.1419G= ENSP00000397937.2:p.Pro473=
ENST00000457475.5:c.1347G= ENSP00000390292.1:p.Pro449=
ENST00000466584.5:n.246G=
ENST00000489429.5:n.1875G=
ENST00000497584.5:n.1670G=
ENST00000523845.5:c.*1074G= ENSP00000428912.1:n.*1074G=
NM_001220.4:c.1791G= NP_001211.3:p.Pro597=
NM_001293170.1:c.1419G= NP_001280099.1:p.Pro473=
NM_172078.2:c.1419G= NP_742075.1:p.Pro473=
NM_172079.2:c.1347G= NP_742076.1:p.Pro449=
NM_172080.2:c.1344G= NP_742077.1:p.Pro448=
NM_172081.2:c.1302G= NP_742078.1:p.Pro434=
NM_172082.2:c.1269G= NP_742079.1:p.Pro423=
NM_172083.2:c.1230G= NP_742080.1:p.Pro410=
NM_172084.2:c.1140G= NP_742081.1:p.Pro380=
XM_005249862.3:c.1374G= XP_005249919.1:p.Pro458=
XM_005249864.3:c.1275G= XP_005249921.1:p.Pro425=
XM_006715781.2:c.1671G= XP_006715844.1:p.Pro557=
XM_006715784.2:c.1347G= XP_006715847.1:p.Pro449=
XM_011515547.1:c.1920G= XP_011513849.1:p.Pro640=
XM_011515548.1:c.1920G= XP_011513850.1:p.Pro640=
XM_011515549.1:c.1875G= XP_011513851.1:p.Pro625=
XM_011515550.1:c.1848G= XP_011513852.1:p.Pro616=
XM_011515551.1:c.1848G= XP_011513853.1:p.Pro616=
XM_011515552.1:c.1845G= XP_011513854.1:p.Pro615=
XM_011515553.1:c.1806G= XP_011513855.1:p.Pro602=
XM_011515554.1:c.1800G= XP_011513856.1:p.Pro600=
XM_011515555.1:c.1791G= XP_011513857.1:p.Pro597=
XM_011515556.1:c.1776G= XP_011513858.1:p.Pro592=
XM_011515557.1:c.1773G= XP_011513859.1:p.Pro591=
XM_011515559.1:c.1533G= XP_011513861.1:p.Pro511=
XM_011515560.1:c.1533G= XP_011513862.1:p.Pro511=
XM_011515559.2:c.1533G= XP_011513861.1:p.Pro511=
XM_017012660.1:c.1803G= XP_016868149.1:p.Pro601=
XM_017012661.1:c.1761G= XP_016868150.1:p.Pro587=
XM_017012662.1:c.1602G= XP_016868151.1:p.Pro534=
XM_017012663.2:c.1461G= XP_016868152.1:p.Pro487=
XM_017012664.1:c.1299G= XP_016868153.1:p.Pro433=
XM_017012665.1:c.1272G= XP_016868154.1:p.Pro424=
XM_017012666.2:c.1032G= XP_016868155.1:p.Pro344=
XM_017012667.2:c.987G= XP_016868156.1:p.Pro329=
XM_017012668.2:c.960G= XP_016868157.1:p.Pro320=
XM_017012669.2:c.960G= XP_016868158.1:p.Pro320=
XM_017012670.2:c.915G= XP_016868159.1:p.Pro305=
XM_024446945.1:c.1677G= XP_024302713.1:p.Pro559=
XM_024446946.1:c.957G= XP_024302714.1:p.Pro319=
NM_001220.5:c.1791G= MANE Select NP_001211.3:p.Pro597=
NM_001293170.2:c.1419G= NP_001280099.1:p.Pro473=
NM_172078.3:c.1419G= NP_742075.1:p.Pro473=
NM_172080.3:c.1344G= NP_742077.1:p.Pro448=
NM_172081.3:c.1302G= NP_742078.1:p.Pro434=
NM_172082.3:c.1269G= NP_742079.1:p.Pro423=
NM_172083.3:c.1230G= NP_742080.1:p.Pro410=
NM_172084.3:c.1140G= NP_742081.1:p.Pro380=
NM_172079.3:c.1347G= NP_742076.1:p.Pro449=