Canonical Allele Identifier: CA411377956

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960859T>A (hg19) ; chr22:g.36564812T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564812T>A , CM000684.2:g.36564812T>A	GRCh38
NC_000022.10:g.36960859T>A , CM000684.1:g.36960859T>A	GRCh37
NC_000022.9:g.35290805T>A	NCBI36
NG_031861.1:g.142832A>T
NG_031861.2:g.143047A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.511A>T MANE Select	ENSP00000300105.6:p.Lys171Ter
ENST00000300105.6:c.511A>T	ENSP00000300105.6:p.Lys171Ter
NM_006078.3:c.511A>T	NP_006069.1:p.Lys171Ter
NM_006078.4:c.511A>T	NP_006069.1:p.Lys171Ter
XM_017028531.2:c.253A>T	XP_016884020.1:p.Lys85Ter
NM_001379051.1:c.442A>T	NP_001365980.1:p.Lys148Ter
NM_006078.5:c.511A>T MANE Select	NP_006069.1:p.Lys171Ter
NR_166440.1:n.1877A>T