Canonical Allele Identifier: CA2403929708

Gene: CACNG2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564875T= , CM000684.2:g.36564875T=	GRCh38
NC_000022.10:g.36960922T= , CM000684.1:g.36960922T=	GRCh37
NC_000022.9:g.35290868T=	NCBI36
NG_031861.1:g.142769A=
NG_031861.2:g.142984A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.448A= MANE Select	ENSP00000300105.6:p.Ile150=
ENST00000300105.6:c.448A=	ENSP00000300105.6:p.Ile150=
NM_006078.3:c.448A=	NP_006069.1:p.Ile150=
NM_006078.4:c.448A=	NP_006069.1:p.Ile150=
XM_017028531.2:c.190A=	XP_016884020.1:p.Ile64=
NM_001379051.1:c.379A=	NP_001365980.1:p.Ile127=
NM_006078.5:c.448A= MANE Select	NP_006069.1:p.Ile150=
NR_166440.1:n.1814A=