Canonical Allele Identifier: CA2403929598
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564587G= , CM000684.2:g.36564587G= GRCh38
NC_000022.10:g.36960634G= , CM000684.1:g.36960634G= GRCh37
NC_000022.9:g.35290580G= NCBI36
NG_031861.1:g.143057C=
NG_031861.2:g.143272C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.736C= MANE Select ENSP00000300105.6:p.Pro246=
ENST00000300105.6:c.736C= ENSP00000300105.6:p.Pro246=
NM_006078.3:c.736C= NP_006069.1:p.Pro246=
NM_006078.4:c.736C= NP_006069.1:p.Pro246=
XM_017028531.2:c.478C= XP_016884020.1:p.Pro160=
NM_001379051.1:c.667C= NP_001365980.1:p.Pro223=
NM_006078.5:c.736C= MANE Select NP_006069.1:p.Pro246=
NR_166440.1:n.2102C=