Canonical Allele Identifier: CA352895525
Gene: GNAI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50256253C>A , CM000665.2:g.50256253C>A GRCh38
NC_000003.11:g.50293685C>A , CM000665.1:g.50293685C>A GRCh37
NC_000003.10:g.50268689C>A NCBI36
NG_016002.2:g.34566C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000313601.11:c.526C>A MANE Select ENSP00000312999.6:p.Leu176Ile
ENST00000266027.9:c.370C>A ENSP00000266027.6:p.Leu124Ile
ENST00000313601.10:c.526C>A ENSP00000312999.6:p.Leu176Ile
ENST00000422163.5:c.478C>A ENSP00000406871.1:p.Leu160Ile
ENST00000440628.5:c.370C>A ENSP00000395736.1:p.Leu124Ile
ENST00000441156.5:c.*54C>A ENSP00000394321.1:n.*54C>A
ENST00000446079.5:c.*161C>A ENSP00000406065.1:n.*161C>A
ENST00000451956.1:c.415C>A ENSP00000406369.1:p.Leu139Ile
ENST00000468422.1:n.93C>A
ENST00000490122.5:n.1353C>A
ENST00000491100.5:n.2342C>A
NM_001166425.1:c.415C>A NP_001159897.1:p.Leu139Ile
NM_001282617.1:c.370C>A NP_001269546.1:p.Leu124Ile
NM_001282618.1:c.283C>A NP_001269547.1:p.Leu95Ile
NM_001282619.1:c.478C>A NP_001269548.1:p.Leu160Ile
NM_001282620.1:c.478C>A NP_001269549.1:p.Leu160Ile
NM_002070.3:c.526C>A NP_002061.1:p.Leu176Ile
NM_002070.4:c.526C>A MANE Select NP_002061.1:p.Leu176Ile
NM_001166425.2:c.415C>A NP_001159897.1:p.Leu139Ile
NM_001282618.2:c.283C>A NP_001269547.1:p.Leu95Ile
NM_001282619.2:c.478C>A NP_001269548.1:p.Leu160Ile
NM_001282620.2:c.478C>A NP_001269549.1:p.Leu160Ile
NM_001282617.2:c.370C>A NP_001269546.1:p.Leu124Ile