Canonical Allele Identifier: CA352895882

Gene: GNAI2

Linked Data

• MyVariant Identifiers: chr3:g.50293727T>A (hg19) ; chr3:g.50256295T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256295T>A , CM000665.2:g.50256295T>A	GRCh38
NC_000003.11:g.50293727T>A , CM000665.1:g.50293727T>A	GRCh37
NC_000003.10:g.50268731T>A	NCBI36
NG_016002.2:g.34608T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.568T>A MANE Select	ENSP00000312999.6:p.Phe190Ile
ENST00000266027.9:c.412T>A	ENSP00000266027.6:p.Phe138Ile
ENST00000313601.10:c.568T>A	ENSP00000312999.6:p.Phe190Ile
ENST00000422163.5:c.520T>A	ENSP00000406871.1:p.Phe174Ile
ENST00000440628.5:c.412T>A	ENSP00000395736.1:p.Phe138Ile
ENST00000441156.5:c.*96T>A	ENSP00000394321.1:n.*96T>A
ENST00000446079.5:c.*203T>A	ENSP00000406065.1:n.*203T>A
ENST00000451956.1:c.457T>A	ENSP00000406369.1:p.Phe153Ile
ENST00000468422.1:n.135T>A
ENST00000490122.5:n.1395T>A
ENST00000491100.5:n.2384T>A
ENST00000492383.1:n.13T>A
NM_001166425.1:c.457T>A	NP_001159897.1:p.Phe153Ile
NM_001282617.1:c.412T>A	NP_001269546.1:p.Phe138Ile
NM_001282618.1:c.325T>A	NP_001269547.1:p.Phe109Ile
NM_001282619.1:c.520T>A	NP_001269548.1:p.Phe174Ile
NM_001282620.1:c.520T>A	NP_001269549.1:p.Phe174Ile
NM_002070.3:c.568T>A	NP_002061.1:p.Phe190Ile
NM_002070.4:c.568T>A MANE Select	NP_002061.1:p.Phe190Ile
NM_001166425.2:c.457T>A	NP_001159897.1:p.Phe153Ile
NM_001282618.2:c.325T>A	NP_001269547.1:p.Phe109Ile
NM_001282619.2:c.520T>A	NP_001269548.1:p.Phe174Ile
NM_001282620.2:c.520T>A	NP_001269549.1:p.Phe174Ile
NM_001282617.2:c.412T>A	NP_001269546.1:p.Phe138Ile