Canonical Allele Identifier: CA2403929662

Gene: CACNG2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564733G= , CM000684.2:g.36564733G=	GRCh38
NC_000022.10:g.36960780G= , CM000684.1:g.36960780G=	GRCh37
NC_000022.9:g.35290726G=	NCBI36
NG_031861.1:g.142911C=
NG_031861.2:g.143126C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.590C= MANE Select	ENSP00000300105.6:p.Ala197=
ENST00000300105.6:c.590C=	ENSP00000300105.6:p.Ala197=
NM_006078.3:c.590C=	NP_006069.1:p.Ala197=
NM_006078.4:c.590C=	NP_006069.1:p.Ala197=
XM_017028531.2:c.332C=	XP_016884020.1:p.Ala111=
NM_001379051.1:c.521C=	NP_001365980.1:p.Ala174=
NM_006078.5:c.590C= MANE Select	NP_006069.1:p.Ala197=
NR_166440.1:n.1956C=