Canonical Allele Identifier: CA2656451646

Gene: CACNG2

Linked Data

• gnomAD v4: 22-36564905-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564905_36564906insA , CM000684.2:g.36564905_36564906insA	GRCh38
NC_000022.10:g.36960952_36960953insA , CM000684.1:g.36960952_36960953insA	GRCh37
NC_000022.9:g.35290898_35290899insA	NCBI36
NG_031861.1:g.142738_142739insT
NG_031861.2:g.142953_142954insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.437-20_437-19insT MANE Select	ENSP00000300105.6:n.437-20_437-19insT
ENST00000300105.6:c.437-20_437-19insT	ENSP00000300105.6:n.437-20_437-19insT
NM_006078.3:c.437-20_437-19insT	NP_006069.1:n.437-20_437-19insT
NM_006078.4:c.437-20_437-19insT	NP_006069.1:n.437-20_437-19insT
XM_017028531.2:c.179-20_179-19insT	XP_016884020.1:n.179-20_179-19insT
NM_001379051.1:c.368-20_368-19insT	NP_001365980.1:n.368-20_368-19insT
NM_006078.5:c.437-20_437-19insT MANE Select	NP_006069.1:n.437-20_437-19insT
NR_166440.1:n.1803-20_1803-19insT