Canonical Allele Identifier: CA338145169
Gene: CAMTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7752473C>G , CM000663.2:g.7752473C>G GRCh38
NC_000001.10:g.7812533C>G , CM000663.1:g.7812533C>G GRCh37
NC_000001.9:g.7735120C>G NCBI36
NG_053148.1:g.972150C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000710284.1:c.1652C>G ENSP00000518174.1:p.Thr551Ser
ENST00000710285.1:c.1991C>G ENSP00000518175.1:p.Thr664Ser
ENST00000476864.2:c.4559C>G ENSP00000452319.2:p.Thr1520Ser
ENST00000495233.6:c.2220C>G
ENST00000700414.1:c.*4431C>G ENSP00000514978.1:n.*4431C>G
ENST00000700415.1:c.4490C>G ENSP00000514979.1:p.Thr1497Ser
ENST00000700417.1:c.4487C>G ENSP00000514981.1:p.Thr1496Ser
ENST00000700419.1:c.2744C>G ENSP00000514983.1:p.Thr915Ser
ENST00000700420.1:c.1949C>G ENSP00000514994.1:p.Thr650Ser
ENST00000700421.1:c.1970C>G ENSP00000514995.1:p.Thr657Ser
ENST00000700422.1:n.1072C>G
ENST00000700423.1:c.1652C>G ENSP00000514996.1:p.Thr551Ser
ENST00000700424.1:c.1652C>G ENSP00000514997.1:p.Thr551Ser
ENST00000700425.1:c.1610C>G ENSP00000514998.1:p.Thr537Ser
ENST00000700445.1:c.2244C>G
ENST00000700446.1:n.3294C>G
ENST00000700447.1:n.2578C>G
ENST00000700448.1:c.582C>G
ENST00000700449.1:c.102C>G
ENST00000303635.12:c.4898C>G MANE Select ENSP00000306522.6:p.Thr1633Ser
ENST00000303635.11:c.4898C>G ENSP00000306522.6:p.Thr1633Ser
ENST00000476864.1:c.590C>G ENSP00000452319.1:p.Thr197Ser
ENST00000490905.5:c.595C>G
ENST00000495233.5:c.1789C>G
NM_015215.3:c.4898C>G NP_056030.1:p.Thr1633Ser
XM_011541083.1:c.4919C>G XP_011539385.1:p.Thr1640Ser
XM_011541084.1:c.4919C>G XP_011539386.1:p.Thr1640Ser
XM_011541085.1:c.4907C>G XP_011539387.1:p.Thr1636Ser
XM_011541086.1:c.4898C>G XP_011539388.1:p.Thr1633Ser
XM_011541087.1:c.4847C>G XP_011539389.1:p.Thr1616Ser
XM_011541088.1:c.4829C>G XP_011539390.1:p.Thr1610Ser
XM_011541089.1:c.4580C>G XP_011539391.1:p.Thr1527Ser
XM_011541090.1:c.4580C>G XP_011539392.1:p.Thr1527Ser
NM_001349608.1:c.4808C>G NP_001336537.1:p.Thr1603Ser
NM_001349609.1:c.4580C>G NP_001336538.1:p.Thr1527Ser
NM_001349610.1:c.4574C>G NP_001336539.1:p.Thr1525Ser
NM_001349612.1:c.4490C>G NP_001336541.1:p.Thr1497Ser
NM_001349613.1:c.2027C>G NP_001336542.1:p.Thr676Ser
NM_001349614.1:c.1991C>G NP_001336543.1:p.Thr664Ser
NM_001349615.1:c.1991C>G NP_001336544.1:p.Thr664Ser
NM_001349616.1:c.1991C>G NP_001336545.1:p.Thr664Ser
NM_001349617.1:c.1970C>G NP_001336546.1:p.Thr657Ser
NM_001349618.1:c.1970C>G NP_001336547.1:p.Thr657Ser
NM_001349619.1:c.1652C>G NP_001336548.1:p.Thr551Ser
NM_001349620.1:c.1652C>G NP_001336549.1:p.Thr551Ser
NM_001349621.1:c.1652C>G NP_001336550.1:p.Thr551Ser
NM_001349622.1:c.1652C>G NP_001336551.1:p.Thr551Ser
NM_001349623.1:c.1631C>G NP_001336552.1:p.Thr544Ser
NM_001349624.2:c.1631C>G NP_001336553.1:p.Thr544Ser
NM_001349625.1:c.1631C>G NP_001336554.1:p.Thr544Ser
NM_001349626.1:c.1631C>G NP_001336555.1:p.Thr544Ser
XM_011541083.2:c.4919C>G XP_011539385.1:p.Thr1640Ser
XM_011541084.2:c.4919C>G XP_011539386.1:p.Thr1640Ser
XM_011541086.3:c.4898C>G XP_011539388.1:p.Thr1633Ser
XM_011541087.2:c.4847C>G XP_011539389.1:p.Thr1616Ser
XM_011541088.2:c.4829C>G XP_011539390.1:p.Thr1610Ser
XM_011541090.3:c.4580C>G XP_011539392.1:p.Thr1527Ser
XM_017000774.2:c.4919C>G XP_016856263.1:p.Thr1640Ser
XM_017000777.1:c.4559C>G XP_016856266.1:p.Thr1520Ser
XM_017000778.1:c.4559C>G XP_016856267.1:p.Thr1520Ser
XM_024454329.1:c.2180C>G XP_024310097.1:p.Thr727Ser
XM_024454330.1:c.2159C>G XP_024310098.1:p.Thr720Ser
XM_024454331.1:c.1991C>G XP_024310099.1:p.Thr664Ser
XM_024454332.1:c.1991C>G XP_024310100.1:p.Thr664Ser
XM_024454333.1:c.1991C>G XP_024310101.1:p.Thr664Ser
XM_024454334.1:c.1991C>G XP_024310102.1:p.Thr664Ser
XM_024454335.1:c.1991C>G XP_024310103.1:p.Thr664Ser
XM_024454338.1:c.1652C>G XP_024310106.1:p.Thr551Ser
NM_015215.4:c.4898C>G MANE Select NP_056030.1:p.Thr1633Ser
NM_001349608.2:c.4808C>G NP_001336537.1:p.Thr1603Ser
NM_001349609.2:c.4580C>G NP_001336538.1:p.Thr1527Ser
NM_001349610.2:c.4574C>G NP_001336539.1:p.Thr1525Ser
NM_001349612.2:c.4490C>G NP_001336541.1:p.Thr1497Ser
NM_001349615.2:c.1991C>G NP_001336544.1:p.Thr664Ser
NM_001349616.2:c.1991C>G NP_001336545.1:p.Thr664Ser
NM_001349618.2:c.1970C>G NP_001336547.1:p.Thr657Ser
NM_001349619.2:c.1652C>G NP_001336548.1:p.Thr551Ser
NM_001349622.2:c.1652C>G NP_001336551.1:p.Thr551Ser
NM_001349624.3:c.1631C>G NP_001336553.1:p.Thr544Ser
NM_001349626.2:c.1631C>G NP_001336555.1:p.Thr544Ser
NM_001349625.2:c.1631C>G NP_001336554.1:p.Thr544Ser