Canonical Allele Identifier: CA352895683
Gene: GNAI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50256275C>A , CM000665.2:g.50256275C>A GRCh38
NC_000003.11:g.50293707C>A , CM000665.1:g.50293707C>A GRCh37
NC_000003.10:g.50268711C>A NCBI36
NG_016002.2:g.34588C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000313601.11:c.548C>A MANE Select ENSP00000312999.6:p.Thr183Lys
ENST00000266027.9:c.392C>A ENSP00000266027.6:p.Thr131Lys
ENST00000313601.10:c.548C>A ENSP00000312999.6:p.Thr183Lys
ENST00000422163.5:c.500C>A ENSP00000406871.1:p.Thr167Lys
ENST00000440628.5:c.392C>A ENSP00000395736.1:p.Thr131Lys
ENST00000441156.5:c.*76C>A ENSP00000394321.1:n.*76C>A
ENST00000446079.5:c.*183C>A ENSP00000406065.1:n.*183C>A
ENST00000451956.1:c.437C>A ENSP00000406369.1:p.Thr146Lys
ENST00000468422.1:n.115C>A
ENST00000490122.5:n.1375C>A
ENST00000491100.5:n.2364C>A
NM_001166425.1:c.437C>A NP_001159897.1:p.Thr146Lys
NM_001282617.1:c.392C>A NP_001269546.1:p.Thr131Lys
NM_001282618.1:c.305C>A NP_001269547.1:p.Thr102Lys
NM_001282619.1:c.500C>A NP_001269548.1:p.Thr167Lys
NM_001282620.1:c.500C>A NP_001269549.1:p.Thr167Lys
NM_002070.3:c.548C>A NP_002061.1:p.Thr183Lys
NM_002070.4:c.548C>A MANE Select NP_002061.1:p.Thr183Lys
NM_001166425.2:c.437C>A NP_001159897.1:p.Thr146Lys
NM_001282618.2:c.305C>A NP_001269547.1:p.Thr102Lys
NM_001282619.2:c.500C>A NP_001269548.1:p.Thr167Lys
NM_001282620.2:c.500C>A NP_001269549.1:p.Thr167Lys
NM_001282617.2:c.392C>A NP_001269546.1:p.Thr131Lys