Canonical Allele Identifier: CA1152049663
Gene: CAMTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7752522C= , CM000663.2:g.7752522C= GRCh38
NC_000001.10:g.7812582C= , CM000663.1:g.7812582C= GRCh37
NC_000001.9:g.7735169C= NCBI36
NG_053148.1:g.972199C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710284.1:c.1701C= ENSP00000518174.1:p.Arg567=
ENST00000710285.1:c.2040C= ENSP00000518175.1:p.Arg680=
ENST00000476864.2:c.4608C= ENSP00000452319.2:p.Arg1536=
ENST00000495233.6:c.2269C=
ENST00000700414.1:c.*4480C= ENSP00000514978.1:n.*4480C=
ENST00000700415.1:c.4539C= ENSP00000514979.1:p.Arg1513=
ENST00000700417.1:c.4536C= ENSP00000514981.1:p.Arg1512=
ENST00000700419.1:c.2793C= ENSP00000514983.1:p.Arg931=
ENST00000700420.1:c.1998C= ENSP00000514994.1:p.Arg666=
ENST00000700421.1:c.2019C= ENSP00000514995.1:p.Arg673=
ENST00000700422.1:n.1121C=
ENST00000700423.1:c.1701C= ENSP00000514996.1:p.Arg567=
ENST00000700424.1:c.1701C= ENSP00000514997.1:p.Arg567=
ENST00000700425.1:c.1659C= ENSP00000514998.1:p.Arg553=
ENST00000700445.1:c.2293C=
ENST00000700446.1:n.3343C=
ENST00000700447.1:n.2627C=
ENST00000700448.1:c.631C=
ENST00000700449.1:c.151C=
ENST00000303635.12:c.4947C= MANE Select ENSP00000306522.6:p.Arg1649=
ENST00000303635.11:c.4947C= ENSP00000306522.6:p.Arg1649=
ENST00000476864.1:c.639C= ENSP00000452319.1:p.Arg213=
ENST00000490905.5:c.644C=
ENST00000495233.5:c.1838C=
NM_015215.3:c.4947C= NP_056030.1:p.Arg1649=
XM_011541083.1:c.4968C= XP_011539385.1:p.Arg1656=
XM_011541084.1:c.4968C= XP_011539386.1:p.Arg1656=
XM_011541085.1:c.4956C= XP_011539387.1:p.Arg1652=
XM_011541086.1:c.4947C= XP_011539388.1:p.Arg1649=
XM_011541087.1:c.4896C= XP_011539389.1:p.Arg1632=
XM_011541088.1:c.4878C= XP_011539390.1:p.Arg1626=
XM_011541089.1:c.4629C= XP_011539391.1:p.Arg1543=
XM_011541090.1:c.4629C= XP_011539392.1:p.Arg1543=
NM_001349608.1:c.4857C= NP_001336537.1:p.Arg1619=
NM_001349609.1:c.4629C= NP_001336538.1:p.Arg1543=
NM_001349610.1:c.4623C= NP_001336539.1:p.Arg1541=
NM_001349612.1:c.4539C= NP_001336541.1:p.Arg1513=
NM_001349613.1:c.2076C= NP_001336542.1:p.Arg692=
NM_001349614.1:c.2040C= NP_001336543.1:p.Arg680=
NM_001349615.1:c.2040C= NP_001336544.1:p.Arg680=
NM_001349616.1:c.2040C= NP_001336545.1:p.Arg680=
NM_001349617.1:c.2019C= NP_001336546.1:p.Arg673=
NM_001349618.1:c.2019C= NP_001336547.1:p.Arg673=
NM_001349619.1:c.1701C= NP_001336548.1:p.Arg567=
NM_001349620.1:c.1701C= NP_001336549.1:p.Arg567=
NM_001349621.1:c.1701C= NP_001336550.1:p.Arg567=
NM_001349622.1:c.1701C= NP_001336551.1:p.Arg567=
NM_001349623.1:c.1680C= NP_001336552.1:p.Arg560=
NM_001349624.2:c.1680C= NP_001336553.1:p.Arg560=
NM_001349625.1:c.1680C= NP_001336554.1:p.Arg560=
NM_001349626.1:c.1680C= NP_001336555.1:p.Arg560=
XM_011541083.2:c.4968C= XP_011539385.1:p.Arg1656=
XM_011541084.2:c.4968C= XP_011539386.1:p.Arg1656=
XM_011541086.3:c.4947C= XP_011539388.1:p.Arg1649=
XM_011541087.2:c.4896C= XP_011539389.1:p.Arg1632=
XM_011541088.2:c.4878C= XP_011539390.1:p.Arg1626=
XM_011541090.3:c.4629C= XP_011539392.1:p.Arg1543=
XM_017000774.2:c.4968C= XP_016856263.1:p.Arg1656=
XM_017000777.1:c.4608C= XP_016856266.1:p.Arg1536=
XM_017000778.1:c.4608C= XP_016856267.1:p.Arg1536=
XM_024454329.1:c.2229C= XP_024310097.1:p.Arg743=
XM_024454330.1:c.2208C= XP_024310098.1:p.Arg736=
XM_024454331.1:c.2040C= XP_024310099.1:p.Arg680=
XM_024454332.1:c.2040C= XP_024310100.1:p.Arg680=
XM_024454333.1:c.2040C= XP_024310101.1:p.Arg680=
XM_024454334.1:c.2040C= XP_024310102.1:p.Arg680=
XM_024454335.1:c.2040C= XP_024310103.1:p.Arg680=
XM_024454338.1:c.1701C= XP_024310106.1:p.Arg567=
NM_015215.4:c.4947C= MANE Select NP_056030.1:p.Arg1649=
NM_001349608.2:c.4857C= NP_001336537.1:p.Arg1619=
NM_001349609.2:c.4629C= NP_001336538.1:p.Arg1543=
NM_001349610.2:c.4623C= NP_001336539.1:p.Arg1541=
NM_001349612.2:c.4539C= NP_001336541.1:p.Arg1513=
NM_001349615.2:c.2040C= NP_001336544.1:p.Arg680=
NM_001349616.2:c.2040C= NP_001336545.1:p.Arg680=
NM_001349618.2:c.2019C= NP_001336547.1:p.Arg673=
NM_001349619.2:c.1701C= NP_001336548.1:p.Arg567=
NM_001349622.2:c.1701C= NP_001336551.1:p.Arg567=
NM_001349624.3:c.1680C= NP_001336553.1:p.Arg560=
NM_001349626.2:c.1680C= NP_001336555.1:p.Arg560=
NM_001349625.2:c.1680C= NP_001336554.1:p.Arg560=