Canonical Allele Identifier: CA338145095
Gene: CAMTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7752464G>C , CM000663.2:g.7752464G>C GRCh38
NC_000001.10:g.7812524G>C , CM000663.1:g.7812524G>C GRCh37
NC_000001.9:g.7735111G>C NCBI36
NG_053148.1:g.972141G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000710284.1:c.1643G>C ENSP00000518174.1:p.Ser548Thr
ENST00000710285.1:c.1982G>C ENSP00000518175.1:p.Ser661Thr
ENST00000476864.2:c.4550G>C ENSP00000452319.2:p.Ser1517Thr
ENST00000495233.6:c.2211G>C
ENST00000700414.1:c.*4422G>C ENSP00000514978.1:n.*4422G>C
ENST00000700415.1:c.4481G>C ENSP00000514979.1:p.Ser1494Thr
ENST00000700417.1:c.4478G>C ENSP00000514981.1:p.Ser1493Thr
ENST00000700419.1:c.2735G>C ENSP00000514983.1:p.Ser912Thr
ENST00000700420.1:c.1940G>C ENSP00000514994.1:p.Ser647Thr
ENST00000700421.1:c.1961G>C ENSP00000514995.1:p.Ser654Thr
ENST00000700422.1:n.1063G>C
ENST00000700423.1:c.1643G>C ENSP00000514996.1:p.Ser548Thr
ENST00000700424.1:c.1643G>C ENSP00000514997.1:p.Ser548Thr
ENST00000700425.1:c.1601G>C ENSP00000514998.1:p.Ser534Thr
ENST00000700445.1:c.2235G>C
ENST00000700446.1:n.3285G>C
ENST00000700447.1:n.2569G>C
ENST00000700448.1:c.574-1G>C
ENST00000700449.1:c.93G>C
ENST00000303635.12:c.4889G>C MANE Select ENSP00000306522.6:p.Ser1630Thr
ENST00000303635.11:c.4889G>C ENSP00000306522.6:p.Ser1630Thr
ENST00000476864.1:c.581G>C ENSP00000452319.1:p.Ser194Thr
ENST00000490905.5:c.586G>C
ENST00000495233.5:c.1780G>C
NM_015215.3:c.4889G>C NP_056030.1:p.Ser1630Thr
XM_011541083.1:c.4910G>C XP_011539385.1:p.Ser1637Thr
XM_011541084.1:c.4910G>C XP_011539386.1:p.Ser1637Thr
XM_011541085.1:c.4898G>C XP_011539387.1:p.Ser1633Thr
XM_011541086.1:c.4889G>C XP_011539388.1:p.Ser1630Thr
XM_011541087.1:c.4838G>C XP_011539389.1:p.Ser1613Thr
XM_011541088.1:c.4820G>C XP_011539390.1:p.Ser1607Thr
XM_011541089.1:c.4571G>C XP_011539391.1:p.Ser1524Thr
XM_011541090.1:c.4571G>C XP_011539392.1:p.Ser1524Thr
NM_001349608.1:c.4799G>C NP_001336537.1:p.Ser1600Thr
NM_001349609.1:c.4571G>C NP_001336538.1:p.Ser1524Thr
NM_001349610.1:c.4566-1G>C NP_001336539.1:n.4566-1G>C
NM_001349612.1:c.4481G>C NP_001336541.1:p.Ser1494Thr
NM_001349613.1:c.2018G>C NP_001336542.1:p.Ser673Thr
NM_001349614.1:c.1982G>C NP_001336543.1:p.Ser661Thr
NM_001349615.1:c.1982G>C NP_001336544.1:p.Ser661Thr
NM_001349616.1:c.1982G>C NP_001336545.1:p.Ser661Thr
NM_001349617.1:c.1961G>C NP_001336546.1:p.Ser654Thr
NM_001349618.1:c.1961G>C NP_001336547.1:p.Ser654Thr
NM_001349619.1:c.1643G>C NP_001336548.1:p.Ser548Thr
NM_001349620.1:c.1643G>C NP_001336549.1:p.Ser548Thr
NM_001349621.1:c.1643G>C NP_001336550.1:p.Ser548Thr
NM_001349622.1:c.1643G>C NP_001336551.1:p.Ser548Thr
NM_001349623.1:c.1622G>C NP_001336552.1:p.Ser541Thr
NM_001349624.2:c.1622G>C NP_001336553.1:p.Ser541Thr
NM_001349625.1:c.1622G>C NP_001336554.1:p.Ser541Thr
NM_001349626.1:c.1622G>C NP_001336555.1:p.Ser541Thr
XM_011541083.2:c.4910G>C XP_011539385.1:p.Ser1637Thr
XM_011541084.2:c.4910G>C XP_011539386.1:p.Ser1637Thr
XM_011541086.3:c.4889G>C XP_011539388.1:p.Ser1630Thr
XM_011541087.2:c.4838G>C XP_011539389.1:p.Ser1613Thr
XM_011541088.2:c.4820G>C XP_011539390.1:p.Ser1607Thr
XM_011541090.3:c.4571G>C XP_011539392.1:p.Ser1524Thr
XM_017000774.2:c.4910G>C XP_016856263.1:p.Ser1637Thr
XM_017000777.1:c.4550G>C XP_016856266.1:p.Ser1517Thr
XM_017000778.1:c.4550G>C XP_016856267.1:p.Ser1517Thr
XM_024454329.1:c.2171G>C XP_024310097.1:p.Ser724Thr
XM_024454330.1:c.2150G>C XP_024310098.1:p.Ser717Thr
XM_024454331.1:c.1982G>C XP_024310099.1:p.Ser661Thr
XM_024454332.1:c.1982G>C XP_024310100.1:p.Ser661Thr
XM_024454333.1:c.1982G>C XP_024310101.1:p.Ser661Thr
XM_024454334.1:c.1982G>C XP_024310102.1:p.Ser661Thr
XM_024454335.1:c.1982G>C XP_024310103.1:p.Ser661Thr
XM_024454338.1:c.1643G>C XP_024310106.1:p.Ser548Thr
NM_015215.4:c.4889G>C MANE Select NP_056030.1:p.Ser1630Thr
NM_001349608.2:c.4799G>C NP_001336537.1:p.Ser1600Thr
NM_001349609.2:c.4571G>C NP_001336538.1:p.Ser1524Thr
NM_001349610.2:c.4566-1G>C NP_001336539.1:n.4566-1G>C
NM_001349612.2:c.4481G>C NP_001336541.1:p.Ser1494Thr
NM_001349615.2:c.1982G>C NP_001336544.1:p.Ser661Thr
NM_001349616.2:c.1982G>C NP_001336545.1:p.Ser661Thr
NM_001349618.2:c.1961G>C NP_001336547.1:p.Ser654Thr
NM_001349619.2:c.1643G>C NP_001336548.1:p.Ser548Thr
NM_001349622.2:c.1643G>C NP_001336551.1:p.Ser548Thr
NM_001349624.3:c.1622G>C NP_001336553.1:p.Ser541Thr
NM_001349626.2:c.1622G>C NP_001336555.1:p.Ser541Thr
NM_001349625.2:c.1622G>C NP_001336554.1:p.Ser541Thr