Canonical Allele Identifier: CA352895169
Gene: GNAI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50256225T>A , CM000665.2:g.50256225T>A GRCh38
NC_000003.11:g.50293657T>A , CM000665.1:g.50293657T>A GRCh37
NC_000003.10:g.50268661T>A NCBI36
NG_016002.2:g.34538T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000313601.11:c.498T>A MANE Select ENSP00000312999.6:p.Ser166Arg
ENST00000266027.9:c.342T>A ENSP00000266027.6:p.Ser114Arg
ENST00000313601.10:c.498T>A ENSP00000312999.6:p.Ser166Arg
ENST00000422163.5:c.450T>A ENSP00000406871.1:p.Ser150Arg
ENST00000440628.5:c.342T>A ENSP00000395736.1:p.Ser114Arg
ENST00000441156.5:c.*26T>A ENSP00000394321.1:n.*26T>A
ENST00000446079.5:c.*133T>A ENSP00000406065.1:n.*133T>A
ENST00000451956.1:c.387T>A ENSP00000406369.1:p.Ser129Arg
ENST00000468422.1:n.65T>A
ENST00000490122.5:n.1325T>A
ENST00000491100.5:n.2314T>A
NM_001166425.1:c.387T>A NP_001159897.1:p.Ser129Arg
NM_001282617.1:c.342T>A NP_001269546.1:p.Ser114Arg
NM_001282618.1:c.255T>A NP_001269547.1:p.Ser85Arg
NM_001282619.1:c.450T>A NP_001269548.1:p.Ser150Arg
NM_001282620.1:c.450T>A NP_001269549.1:p.Ser150Arg
NM_002070.3:c.498T>A NP_002061.1:p.Ser166Arg
NM_002070.4:c.498T>A MANE Select NP_002061.1:p.Ser166Arg
NM_001166425.2:c.387T>A NP_001159897.1:p.Ser129Arg
NM_001282618.2:c.255T>A NP_001269547.1:p.Ser85Arg
NM_001282619.2:c.450T>A NP_001269548.1:p.Ser150Arg
NM_001282620.2:c.450T>A NP_001269549.1:p.Ser150Arg
NM_001282617.2:c.342T>A NP_001269546.1:p.Ser114Arg