Canonical Allele Identifier: CA1025473036

Gene: CACNG2

Linked Data

• gnomAD v3: 22-36701523-A-ACCCCCC
• gnomAD v4: 22-36701523-A-ACCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36701525_36701526insCCCCCC , CM000684.2:g.36701525_36701526insCCCCCC	GRCh38
NC_000022.10:g.37097570_37097571insCCCCCC , CM000684.1:g.37097570_37097571insCCCCCC	GRCh37
NC_000022.9:g.35427516_35427517insCCCCCC	NCBI36
NG_031861.1:g.6122_6123insGGGGGG
NG_031861.2:g.6335_6336insGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.211+842_211+843insGGGGGG MANE Select	ENSP00000300105.6:n.211+842_211+843insGGGGGG
ENST00000300105.6:c.211+842_211+843insGGGGGG	ENSP00000300105.6:n.211+842_211+843insGGGGGG
NM_006078.3:c.211+842_211+843insGGGGGG	NP_006069.1:n.211+842_211+843insGGGGGG
NM_006078.4:c.211+842_211+843insGGGGGG	NP_006069.1:n.211+842_211+843insGGGGGG
NM_001379051.1:c.142+842_142+843insGGGGGG	NP_001365980.1:n.142+842_142+843insGGGGGG
NM_006078.5:c.211+842_211+843insGGGGGG MANE Select	NP_006069.1:n.211+842_211+843insGGGGGG
NR_166440.1:n.1387+842_1387+843insGGGGGG