Canonical Allele Identifier: CA433694939

Gene: GNAI2

Linked Data

• dbSNP Id: rs1700700798
• COSMIC: COSM1291732
• MyVariant Identifiers: chr3:g.50293687A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256255A>G , CM000665.2:g.50256255A>G	GRCh38
NC_000003.11:g.50293687A>G , CM000665.1:g.50293687A>G	GRCh37
NC_000003.10:g.50268691A>G	NCBI36
NG_016002.2:g.34568A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.528A>G MANE Select	ENSP00000312999.6:p.Leu176=
ENST00000266027.9:c.372A>G	ENSP00000266027.6:p.Leu124=
ENST00000313601.10:c.528A>G	ENSP00000312999.6:p.Leu176=
ENST00000422163.5:c.480A>G	ENSP00000406871.1:p.Leu160=
ENST00000440628.5:c.372A>G	ENSP00000395736.1:p.Leu124=
ENST00000441156.5:c.*56A>G	ENSP00000394321.1:n.*56A>G
ENST00000446079.5:c.*163A>G	ENSP00000406065.1:n.*163A>G
ENST00000451956.1:c.417A>G	ENSP00000406369.1:p.Leu139=
ENST00000468422.1:n.95A>G
ENST00000490122.5:n.1355A>G
ENST00000491100.5:n.2344A>G
NM_001166425.1:c.417A>G	NP_001159897.1:p.Leu139=
NM_001282617.1:c.372A>G	NP_001269546.1:p.Leu124=
NM_001282618.1:c.285A>G	NP_001269547.1:p.Leu95=
NM_001282619.1:c.480A>G	NP_001269548.1:p.Leu160=
NM_001282620.1:c.480A>G	NP_001269549.1:p.Leu160=
NM_002070.3:c.528A>G	NP_002061.1:p.Leu176=
NM_002070.4:c.528A>G MANE Select	NP_002061.1:p.Leu176=
NM_001166425.2:c.417A>G	NP_001159897.1:p.Leu139=
NM_001282618.2:c.285A>G	NP_001269547.1:p.Leu95=
NM_001282619.2:c.480A>G	NP_001269548.1:p.Leu160=
NM_001282620.2:c.480A>G	NP_001269549.1:p.Leu160=
NM_001282617.2:c.372A>G	NP_001269546.1:p.Leu124=