Canonical Allele Identifier: CA383799469

Gene: C3AR1

Linked Data

• gnomAD v4: 12-8059843-C-T
• COSMIC: COSM3987233
• MyVariant Identifiers: chr12:g.8212439C>T (hg19) ; chr12:g.8059843C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8059843C>T , CM000674.2:g.8059843C>T	GRCh38
NC_000012.11:g.8212439C>T , CM000674.1:g.8212439C>T	GRCh37
NC_000012.10:g.8103706C>T	NCBI36
NG_050736.1:g.11629G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307637.5:c.343G>A MANE Select	ENSP00000302079.4:p.Ala115Thr
ENST00000307637.4:c.343G>A	ENSP00000302079.4:p.Ala115Thr
ENST00000546241.1:c.343G>A	ENSP00000444500.1:p.Ala115Thr
NM_004054.2:c.343G>A	NP_004045.1:p.Ala115Thr
NM_001326475.1:c.343G>A	NP_001313404.1:p.Ala115Thr
NM_001326477.1:c.343G>A	NP_001313406.1:p.Ala115Thr
NM_004054.3:c.343G>A	NP_004045.1:p.Ala115Thr
NM_001326475.2:c.343G>A	NP_001313404.1:p.Ala115Thr
NM_001326477.2:c.343G>A	NP_001313406.1:p.Ala115Thr
NM_004054.4:c.343G>A MANE Select	NP_004045.1:p.Ala115Thr