Canonical Allele Identifier: CA352895316

Gene: GNAI2

Linked Data

• COSMIC: COSM1046445
• MyVariant Identifiers: chr3:g.50293670A>G (hg19) ; chr3:g.50256238A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256238A>G , CM000665.2:g.50256238A>G	GRCh38
NC_000003.11:g.50293670A>G , CM000665.1:g.50293670A>G	GRCh37
NC_000003.10:g.50268674A>G	NCBI36
NG_016002.2:g.34551A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.511A>G MANE Select	ENSP00000312999.6:p.Thr171Ala
ENST00000266027.9:c.355A>G	ENSP00000266027.6:p.Thr119Ala
ENST00000313601.10:c.511A>G	ENSP00000312999.6:p.Thr171Ala
ENST00000422163.5:c.463A>G	ENSP00000406871.1:p.Thr155Ala
ENST00000440628.5:c.355A>G	ENSP00000395736.1:p.Thr119Ala
ENST00000441156.5:c.*39A>G	ENSP00000394321.1:n.*39A>G
ENST00000446079.5:c.*146A>G	ENSP00000406065.1:n.*146A>G
ENST00000451956.1:c.400A>G	ENSP00000406369.1:p.Thr134Ala
ENST00000468422.1:n.78A>G
ENST00000490122.5:n.1338A>G
ENST00000491100.5:n.2327A>G
NM_001166425.1:c.400A>G	NP_001159897.1:p.Thr134Ala
NM_001282617.1:c.355A>G	NP_001269546.1:p.Thr119Ala
NM_001282618.1:c.268A>G	NP_001269547.1:p.Thr90Ala
NM_001282619.1:c.463A>G	NP_001269548.1:p.Thr155Ala
NM_001282620.1:c.463A>G	NP_001269549.1:p.Thr155Ala
NM_002070.3:c.511A>G	NP_002061.1:p.Thr171Ala
NM_002070.4:c.511A>G MANE Select	NP_002061.1:p.Thr171Ala
NM_001166425.2:c.400A>G	NP_001159897.1:p.Thr134Ala
NM_001282618.2:c.268A>G	NP_001269547.1:p.Thr90Ala
NM_001282619.2:c.463A>G	NP_001269548.1:p.Thr155Ala
NM_001282620.2:c.463A>G	NP_001269549.1:p.Thr155Ala
NM_001282617.2:c.355A>G	NP_001269546.1:p.Thr119Ala