Canonical Allele Identifier: CA411376026

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960635C>A (hg19) ; chr22:g.36564588C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564588C>A , CM000684.2:g.36564588C>A	GRCh38
NC_000022.10:g.36960635C>A , CM000684.1:g.36960635C>A	GRCh37
NC_000022.9:g.35290581C>A	NCBI36
NG_031861.1:g.143056G>T
NG_031861.2:g.143271G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.735G>T MANE Select	ENSP00000300105.6:p.Glu245Asp
ENST00000300105.6:c.735G>T	ENSP00000300105.6:p.Glu245Asp
NM_006078.3:c.735G>T	NP_006069.1:p.Glu245Asp
NM_006078.4:c.735G>T	NP_006069.1:p.Glu245Asp
XM_017028531.2:c.477G>T	XP_016884020.1:p.Glu159Asp
NM_001379051.1:c.666G>T	NP_001365980.1:p.Glu222Asp
NM_006078.5:c.735G>T MANE Select	NP_006069.1:p.Glu245Asp
NR_166440.1:n.2101G>T