Canonical Allele Identifier: CA2405415116

Gene: CACNA1I

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.39679397G= , CM000684.2:g.39679397G=	GRCh38
NC_000022.10:g.40075402G= , CM000684.1:g.40075402G=	GRCh37
NC_000022.9:g.38405348G=	NCBI36
NG_052947.1:g.113645G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000402142.4:c.5346G= MANE Select	ENSP00000385019.3:p.Gly1782=
ENST00000401624.5:c.5346G=	ENSP00000383887.1:p.Gly1782=
ENST00000402142.3:c.5346G=	ENSP00000385019.3:p.Gly1782=
ENST00000404898.5:c.5241G=	ENSP00000384093.1:p.Gly1747=
ENST00000407673.5:c.5241G=	ENSP00000385680.1:p.Gly1747=
NM_001003406.1:c.5241G=	NP_001003406.1:p.Gly1747=
NM_021096.3:c.5346G=	NP_066919.2:p.Gly1782=
XM_011530480.1:c.5241G=	XP_011528782.1:p.Gly1747=
XM_011530481.1:c.5241G=	XP_011528783.1:p.Gly1747=
XM_017029035.2:c.3492G=	XP_016884524.1:p.Gly1164=
XM_017029036.1:c.3492G=	XP_016884525.1:p.Gly1164=
XM_017029037.1:c.3492G=	XP_016884526.1:p.Gly1164=
NM_001003406.2:c.5241G=	NP_001003406.1:p.Gly1747=
NM_021096.4:c.5346G= MANE Select	NP_066919.2:p.Gly1782=