Canonical Allele Identifier: CA2656451692

Gene: CACNG2

Linked Data

• gnomAD v4: 22-36564964-C-CGTAAAGGACGGGGACAGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564967_36564985dup , CM000684.2:g.36564967_36564985dup	GRCh38
NC_000022.10:g.36961014_36961032dup , CM000684.1:g.36961014_36961032dup	GRCh37
NC_000022.9:g.35290960_35290978dup	NCBI36
NG_031861.1:g.142661_142679dup
NG_031861.2:g.142876_142894dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.437-97_437-79dup MANE Select	ENSP00000300105.6:n.437-97_437-79dup
ENST00000300105.6:c.437-97_437-79dup	ENSP00000300105.6:n.437-97_437-79dup
NM_006078.3:c.437-97_437-79dup	NP_006069.1:n.437-97_437-79dup
NM_006078.4:c.437-97_437-79dup	NP_006069.1:n.437-97_437-79dup
XM_017028531.2:c.179-97_179-79dup	XP_016884020.1:n.179-97_179-79dup
NM_001379051.1:c.368-97_368-79dup	NP_001365980.1:n.368-97_368-79dup
NM_006078.5:c.437-97_437-79dup MANE Select	NP_006069.1:n.437-97_437-79dup
NR_166440.1:n.1803-97_1803-79dup