Canonical Allele Identifier: CA1152049668

Gene: CAMTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7752526C= , CM000663.2:g.7752526C=	GRCh38
NC_000001.10:g.7812586C= , CM000663.1:g.7812586C=	GRCh37
NC_000001.9:g.7735173C=	NCBI36
NG_053148.1:g.972203C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710284.1:c.1705C=	ENSP00000518174.1:p.Arg569=
ENST00000710285.1:c.2044C=	ENSP00000518175.1:p.Arg682=
ENST00000476864.2:c.4612C=	ENSP00000452319.2:p.Arg1538=
ENST00000495233.6:c.2273C=
ENST00000700414.1:c.*4484C=	ENSP00000514978.1:n.*4484C=
ENST00000700415.1:c.4543C=	ENSP00000514979.1:p.Arg1515=
ENST00000700417.1:c.4540C=	ENSP00000514981.1:p.Arg1514=
ENST00000700419.1:c.2797C=	ENSP00000514983.1:p.Arg933=
ENST00000700420.1:c.2002C=	ENSP00000514994.1:p.Arg668=
ENST00000700421.1:c.2023C=	ENSP00000514995.1:p.Arg675=
ENST00000700422.1:n.1125C=
ENST00000700423.1:c.1705C=	ENSP00000514996.1:p.Arg569=
ENST00000700424.1:c.1705C=	ENSP00000514997.1:p.Arg569=
ENST00000700425.1:c.1663C=	ENSP00000514998.1:p.Arg555=
ENST00000700445.1:c.2297C=
ENST00000700446.1:n.3347C=
ENST00000700447.1:n.2631C=
ENST00000700448.1:c.635C=
ENST00000700449.1:c.155C=
ENST00000303635.12:c.4951C= MANE Select	ENSP00000306522.6:p.Arg1651=
ENST00000303635.11:c.4951C=	ENSP00000306522.6:p.Arg1651=
ENST00000476864.1:c.643C=	ENSP00000452319.1:p.Arg215=
ENST00000490905.5:c.648C=
ENST00000495233.5:c.1842C=
NM_015215.3:c.4951C=	NP_056030.1:p.Arg1651=
XM_011541083.1:c.4972C=	XP_011539385.1:p.Arg1658=
XM_011541084.1:c.4972C=	XP_011539386.1:p.Arg1658=
XM_011541085.1:c.4960C=	XP_011539387.1:p.Arg1654=
XM_011541086.1:c.4951C=	XP_011539388.1:p.Arg1651=
XM_011541087.1:c.4900C=	XP_011539389.1:p.Arg1634=
XM_011541088.1:c.4882C=	XP_011539390.1:p.Arg1628=
XM_011541089.1:c.4633C=	XP_011539391.1:p.Arg1545=
XM_011541090.1:c.4633C=	XP_011539392.1:p.Arg1545=
NM_001349608.1:c.4861C=	NP_001336537.1:p.Arg1621=
NM_001349609.1:c.4633C=	NP_001336538.1:p.Arg1545=
NM_001349610.1:c.4627C=	NP_001336539.1:p.Arg1543=
NM_001349612.1:c.4543C=	NP_001336541.1:p.Arg1515=
NM_001349613.1:c.2080C=	NP_001336542.1:p.Arg694=
NM_001349614.1:c.2044C=	NP_001336543.1:p.Arg682=
NM_001349615.1:c.2044C=	NP_001336544.1:p.Arg682=
NM_001349616.1:c.2044C=	NP_001336545.1:p.Arg682=
NM_001349617.1:c.2023C=	NP_001336546.1:p.Arg675=
NM_001349618.1:c.2023C=	NP_001336547.1:p.Arg675=
NM_001349619.1:c.1705C=	NP_001336548.1:p.Arg569=
NM_001349620.1:c.1705C=	NP_001336549.1:p.Arg569=
NM_001349621.1:c.1705C=	NP_001336550.1:p.Arg569=
NM_001349622.1:c.1705C=	NP_001336551.1:p.Arg569=
NM_001349623.1:c.1684C=	NP_001336552.1:p.Arg562=
NM_001349624.2:c.1684C=	NP_001336553.1:p.Arg562=
NM_001349625.1:c.1684C=	NP_001336554.1:p.Arg562=
NM_001349626.1:c.1684C=	NP_001336555.1:p.Arg562=
XM_011541083.2:c.4972C=	XP_011539385.1:p.Arg1658=
XM_011541084.2:c.4972C=	XP_011539386.1:p.Arg1658=
XM_011541086.3:c.4951C=	XP_011539388.1:p.Arg1651=
XM_011541087.2:c.4900C=	XP_011539389.1:p.Arg1634=
XM_011541088.2:c.4882C=	XP_011539390.1:p.Arg1628=
XM_011541090.3:c.4633C=	XP_011539392.1:p.Arg1545=
XM_017000774.2:c.4972C=	XP_016856263.1:p.Arg1658=
XM_017000777.1:c.4612C=	XP_016856266.1:p.Arg1538=
XM_017000778.1:c.4612C=	XP_016856267.1:p.Arg1538=
XM_024454329.1:c.2233C=	XP_024310097.1:p.Arg745=
XM_024454330.1:c.2212C=	XP_024310098.1:p.Arg738=
XM_024454331.1:c.2044C=	XP_024310099.1:p.Arg682=
XM_024454332.1:c.2044C=	XP_024310100.1:p.Arg682=
XM_024454333.1:c.2044C=	XP_024310101.1:p.Arg682=
XM_024454334.1:c.2044C=	XP_024310102.1:p.Arg682=
XM_024454335.1:c.2044C=	XP_024310103.1:p.Arg682=
XM_024454338.1:c.1705C=	XP_024310106.1:p.Arg569=
NM_015215.4:c.4951C= MANE Select	NP_056030.1:p.Arg1651=
NM_001349608.2:c.4861C=	NP_001336537.1:p.Arg1621=
NM_001349609.2:c.4633C=	NP_001336538.1:p.Arg1545=
NM_001349610.2:c.4627C=	NP_001336539.1:p.Arg1543=
NM_001349612.2:c.4543C=	NP_001336541.1:p.Arg1515=
NM_001349615.2:c.2044C=	NP_001336544.1:p.Arg682=
NM_001349616.2:c.2044C=	NP_001336545.1:p.Arg682=
NM_001349618.2:c.2023C=	NP_001336547.1:p.Arg675=
NM_001349619.2:c.1705C=	NP_001336548.1:p.Arg569=
NM_001349622.2:c.1705C=	NP_001336551.1:p.Arg569=
NM_001349624.3:c.1684C=	NP_001336553.1:p.Arg562=
NM_001349626.2:c.1684C=	NP_001336555.1:p.Arg562=
NM_001349625.2:c.1684C=	NP_001336554.1:p.Arg562=