Canonical Allele Identifier: CA2656451639

Gene: CACNG2

Linked Data

• gnomAD v4: 22-36564897-CAGGGTGGCGGGGTGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564898_36564912del , CM000684.2:g.36564898_36564912del	GRCh38
NC_000022.10:g.36960945_36960959del , CM000684.1:g.36960945_36960959del	GRCh37
NC_000022.9:g.35290891_35290905del	NCBI36
NG_031861.1:g.142732_142746del
NG_031861.2:g.142947_142961del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.437-26_437-12del MANE Select	ENSP00000300105.6:n.437-26_437-12del
ENST00000300105.6:c.437-26_437-12del	ENSP00000300105.6:n.437-26_437-12del
NM_006078.3:c.437-26_437-12del	NP_006069.1:n.437-26_437-12del
NM_006078.4:c.437-26_437-12del	NP_006069.1:n.437-26_437-12del
XM_017028531.2:c.179-26_179-12del	XP_016884020.1:n.179-26_179-12del
NM_001379051.1:c.368-26_368-12del	NP_001365980.1:n.368-26_368-12del
NM_006078.5:c.437-26_437-12del MANE Select	NP_006069.1:n.437-26_437-12del
NR_166440.1:n.1803-26_1803-12del