Canonical Allele Identifier: CA2403929606
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564606G= , CM000684.2:g.36564606G= GRCh38
NC_000022.10:g.36960653G= , CM000684.1:g.36960653G= GRCh37
NC_000022.9:g.35290599G= NCBI36
NG_031861.1:g.143038C=
NG_031861.2:g.143253C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.717C= MANE Select ENSP00000300105.6:p.Ser239=
ENST00000300105.6:c.717C= ENSP00000300105.6:p.Ser239=
NM_006078.3:c.717C= NP_006069.1:p.Ser239=
NM_006078.4:c.717C= NP_006069.1:p.Ser239=
XM_017028531.2:c.459C= XP_016884020.1:p.Ser153=
NM_001379051.1:c.648C= NP_001365980.1:p.Ser216=
NM_006078.5:c.717C= MANE Select NP_006069.1:p.Ser239=
NR_166440.1:n.2083C=