Canonical Allele Identifier: CA2403929743
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564939C= , CM000684.2:g.36564939C= GRCh38
NC_000022.10:g.36960986C= , CM000684.1:g.36960986C= GRCh37
NC_000022.9:g.35290932C= NCBI36
NG_031861.1:g.142705G=
NG_031861.2:g.142920G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.437-53G= MANE Select ENSP00000300105.6:n.437-53G=
ENST00000300105.6:c.437-53G= ENSP00000300105.6:n.437-53G=
NM_006078.3:c.437-53G= NP_006069.1:n.437-53G=
NM_006078.4:c.437-53G= NP_006069.1:n.437-53G=
XM_017028531.2:c.179-53G= XP_016884020.1:n.179-53G=
NM_001379051.1:c.368-53G= NP_001365980.1:n.368-53G=
NM_006078.5:c.437-53G= MANE Select NP_006069.1:n.437-53G=
NR_166440.1:n.1803-53G=