Canonical Allele Identifier: CA2403929599
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564588C= , CM000684.2:g.36564588C= GRCh38
NC_000022.10:g.36960635C= , CM000684.1:g.36960635C= GRCh37
NC_000022.9:g.35290581C= NCBI36
NG_031861.1:g.143056G=
NG_031861.2:g.143271G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.735G= MANE Select ENSP00000300105.6:p.Glu245=
ENST00000300105.6:c.735G= ENSP00000300105.6:p.Glu245=
NM_006078.3:c.735G= NP_006069.1:p.Glu245=
NM_006078.4:c.735G= NP_006069.1:p.Glu245=
XM_017028531.2:c.477G= XP_016884020.1:p.Glu159=
NM_001379051.1:c.666G= NP_001365980.1:p.Glu222=
NM_006078.5:c.735G= MANE Select NP_006069.1:p.Glu245=
NR_166440.1:n.2101G=