Canonical Allele Identifier: CA1211176537

Gene: CACNA1E

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.181651536T= , CM000663.2:g.181651536T=	GRCh38
NC_000001.10:g.181620672T= , CM000663.1:g.181620672T=	GRCh37
NC_000001.9:g.179887295T=	NCBI36
NG_050616.1:g.173226T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367570.6:c.1055+95T=	ENSP00000356542.1:n.1055+95T=
ENST00000700187.1:n.1037+95T=
ENST00000367573.7:c.1055+95T= MANE Select	ENSP00000356545.2:n.1055+95T=
ENST00000524607.6:c.1490+95T=	ENSP00000432038.2:n.1490+95T=
ENST00000357570.9:c.1055+95T=	ENSP00000350183.6:n.1055+95T=
ENST00000358338.7:c.1055+95T=	ENSP00000351101.6:n.1055+95T=
ENST00000360108.7:c.1055+95T=	ENSP00000353222.3:n.1055+95T=
ENST00000367567.8:c.1055+95T=	ENSP00000356539.5:n.1055+95T=
ENST00000367570.5:c.1055+95T=	ENSP00000356542.1:n.1055+95T=
ENST00000367573.6:c.1055+95T=	ENSP00000356545.2:n.1055+95T=
ENST00000524607.5:c.1055+95T=	ENSP00000432038.1:n.1055+95T=
ENST00000533229.1:n.1584T=
ENST00000621551.3:c.1055+95T=	ENSP00000483914.1:n.1055+95T=
ENST00000621791.4:c.1055+95T=	ENSP00000481619.1:n.1055+95T=
NM_000721.3:c.1055+95T=	NP_000712.2:n.1055+95T=
NM_001205293.1:c.1055+95T=	NP_001192222.1:n.1055+95T=
NM_001205294.1:c.1055+95T=	NP_001192223.1:n.1055+95T=
XM_011509971.1:c.1055+95T=	XP_011508273.1:n.1055+95T=
NM_001205293.2:c.1055+95T=	NP_001192222.1:n.1055+95T=
XM_017002243.1:c.1490+95T=	XP_016857732.1:n.1490+95T=
XM_017002244.1:c.1490+95T=	XP_016857733.1:n.1490+95T=
XM_017002245.1:c.1490+95T=	XP_016857734.1:n.1490+95T=
XM_017002246.1:c.1490+95T=	XP_016857735.1:n.1490+95T=
XM_017002247.1:c.1490+95T=	XP_016857736.1:n.1490+95T=
XM_017002248.1:c.1490+95T=	XP_016857737.1:n.1490+95T=
XM_017002249.1:c.1490+95T=	XP_016857738.1:n.1490+95T=
XM_017002250.1:c.1490+95T=	XP_016857739.1:n.1490+95T=
XM_017002251.1:c.1490+95T=	XP_016857740.1:n.1490+95T=
NM_001205293.3:c.1055+95T= MANE Select	NP_001192222.1:n.1055+95T=
NM_000721.4:c.1055+95T=	NP_000712.2:n.1055+95T=
NM_001205294.2:c.1055+95T=	NP_001192223.1:n.1055+95T=