Canonical Allele Identifier: CA2656451726

Gene: CACNG2

Linked Data

• gnomAD v4: 22-36564994-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564998del , CM000684.2:g.36564998del	GRCh38
NC_000022.10:g.36961045del , CM000684.1:g.36961045del	GRCh37
NC_000022.9:g.35290991del	NCBI36
NG_031861.1:g.142649del
NG_031861.2:g.142864del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.437-109del MANE Select	ENSP00000300105.6:n.437-109del
ENST00000300105.6:c.437-109del	ENSP00000300105.6:n.437-109del
NM_006078.3:c.437-109del	NP_006069.1:n.437-109del
NM_006078.4:c.437-109del	NP_006069.1:n.437-109del
XM_017028531.2:c.179-109del	XP_016884020.1:n.179-109del
NM_001379051.1:c.368-109del	NP_001365980.1:n.368-109del
NM_006078.5:c.437-109del MANE Select	NP_006069.1:n.437-109del
NR_166440.1:n.1803-109del