Canonical Allele Identifier: CA352896110

Gene: GNAI2

Linked Data

• MyVariant Identifiers: chr3:g.50293748T>A (hg19) ; chr3:g.50256316T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256316T>A , CM000665.2:g.50256316T>A	GRCh38
NC_000003.11:g.50293748T>A , CM000665.1:g.50293748T>A	GRCh37
NC_000003.10:g.50268752T>A	NCBI36
NG_016002.2:g.34629T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.589T>A MANE Select	ENSP00000312999.6:p.Phe197Ile
ENST00000266027.9:c.433T>A	ENSP00000266027.6:p.Phe145Ile
ENST00000313601.10:c.589T>A	ENSP00000312999.6:p.Phe197Ile
ENST00000422163.5:c.541T>A	ENSP00000406871.1:p.Phe181Ile
ENST00000440628.5:c.433T>A	ENSP00000395736.1:p.Phe145Ile
ENST00000441156.5:c.*117T>A	ENSP00000394321.1:n.*117T>A
ENST00000446079.5:c.*224T>A	ENSP00000406065.1:n.*224T>A
ENST00000451956.1:c.478T>A	ENSP00000406369.1:p.Phe160Ile
ENST00000468422.1:n.156T>A
ENST00000490122.5:n.1416T>A
ENST00000491100.5:n.2405T>A
ENST00000492383.1:n.34T>A
NM_001166425.1:c.478T>A	NP_001159897.1:p.Phe160Ile
NM_001282617.1:c.433T>A	NP_001269546.1:p.Phe145Ile
NM_001282618.1:c.346T>A	NP_001269547.1:p.Phe116Ile
NM_001282619.1:c.541T>A	NP_001269548.1:p.Phe181Ile
NM_001282620.1:c.541T>A	NP_001269549.1:p.Phe181Ile
NM_002070.3:c.589T>A	NP_002061.1:p.Phe197Ile
NM_002070.4:c.589T>A MANE Select	NP_002061.1:p.Phe197Ile
NM_001166425.2:c.478T>A	NP_001159897.1:p.Phe160Ile
NM_001282618.2:c.346T>A	NP_001269547.1:p.Phe116Ile
NM_001282619.2:c.541T>A	NP_001269548.1:p.Phe181Ile
NM_001282620.2:c.541T>A	NP_001269549.1:p.Phe181Ile
NM_001282617.2:c.433T>A	NP_001269546.1:p.Phe145Ile