Canonical Allele Identifier: CA2403994199

Gene: CACNG2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36701530_36701533delinsCATG , CM000684.2:g.36701530_36701533delinsCATG	GRCh38
NC_000022.10:g.37097575_37097578delinsCATG , CM000684.1:g.37097575_37097578delinsCATG	GRCh37
NC_000022.9:g.35427521_35427524delinsCATG	NCBI36
NG_031861.1:g.6113_6116delinsCATG
NG_031861.2:g.6326_6329delinsCATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.211+833_211+836delinsCATG MANE Select	ENSP00000300105.6:n.211+833_211+836delinsCATG
ENST00000300105.6:c.211+833_211+836delinsCATG	ENSP00000300105.6:n.211+833_211+836delinsCATG
NM_006078.3:c.211+833_211+836delinsCATG	NP_006069.1:n.211+833_211+836delinsCATG
NM_006078.4:c.211+833_211+836delinsCATG	NP_006069.1:n.211+833_211+836delinsCATG
NM_001379051.1:c.142+833_142+836delinsCATG	NP_001365980.1:n.142+833_142+836delinsCATG
NM_006078.5:c.211+833_211+836delinsCATG MANE Select	NP_006069.1:n.211+833_211+836delinsCATG
NR_166440.1:n.1387+833_1387+836delinsCATG