Canonical Allele Identifier: CA2818892109

Gene: CACNG2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36701530_36701531insCAGGCC , CM000684.2:g.36701530_36701531insCAGGCC	GRCh38
NC_000022.10:g.37097575_37097576insCAGGCC , CM000684.1:g.37097575_37097576insCAGGCC	GRCh37
NC_000022.9:g.35427521_35427522insCAGGCC	NCBI36
NG_031861.1:g.6117_6118insCCTGGG
NG_031861.2:g.6330_6331insCCTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.211+837_211+838insCCTGGG MANE Select	ENSP00000300105.6:n.211+837_211+838insCCTGGG
ENST00000300105.6:c.211+837_211+838insCCTGGG	ENSP00000300105.6:n.211+837_211+838insCCTGGG
NM_006078.3:c.211+837_211+838insCCTGGG	NP_006069.1:n.211+837_211+838insCCTGGG
NM_006078.4:c.211+837_211+838insCCTGGG	NP_006069.1:n.211+837_211+838insCCTGGG
NM_001379051.1:c.142+837_142+838insCCTGGG	NP_001365980.1:n.142+837_142+838insCCTGGG
NM_006078.5:c.211+837_211+838insCCTGGG MANE Select	NP_006069.1:n.211+837_211+838insCCTGGG
NR_166440.1:n.1387+837_1387+838insCCTGGG