Canonical Allele Identifier: CA2403929618

Gene: CACNG2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564632A= , CM000684.2:g.36564632A=	GRCh38
NC_000022.10:g.36960679A= , CM000684.1:g.36960679A=	GRCh37
NC_000022.9:g.35290625A=	NCBI36
NG_031861.1:g.143012T=
NG_031861.2:g.143227T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.691T= MANE Select	ENSP00000300105.6:p.Tyr231=
ENST00000300105.6:c.691T=	ENSP00000300105.6:p.Tyr231=
NM_006078.3:c.691T=	NP_006069.1:p.Tyr231=
NM_006078.4:c.691T=	NP_006069.1:p.Tyr231=
XM_017028531.2:c.433T=	XP_016884020.1:p.Tyr145=
NM_001379051.1:c.622T=	NP_001365980.1:p.Tyr208=
NM_006078.5:c.691T= MANE Select	NP_006069.1:p.Tyr231=
NR_166440.1:n.2057T=