Canonical Allele Identifier: CA352895100
Gene: GNAI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50256221A>T , CM000665.2:g.50256221A>T GRCh38
NC_000003.11:g.50293653A>T , CM000665.1:g.50293653A>T GRCh37
NC_000003.10:g.50268657A>T NCBI36
NG_016002.2:g.34534A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000313601.11:c.494A>T MANE Select ENSP00000312999.6:p.Gln165Leu
ENST00000266027.9:c.338A>T ENSP00000266027.6:p.Gln113Leu
ENST00000313601.10:c.494A>T ENSP00000312999.6:p.Gln165Leu
ENST00000422163.5:c.446A>T ENSP00000406871.1:p.Gln149Leu
ENST00000440628.5:c.338A>T ENSP00000395736.1:p.Gln113Leu
ENST00000441156.5:c.*22A>T ENSP00000394321.1:n.*22A>T
ENST00000446079.5:c.*129A>T ENSP00000406065.1:n.*129A>T
ENST00000451956.1:c.383A>T ENSP00000406369.1:p.Gln128Leu
ENST00000468422.1:n.61A>T
ENST00000490122.5:n.1321A>T
ENST00000491100.5:n.2310A>T
NM_001166425.1:c.383A>T NP_001159897.1:p.Gln128Leu
NM_001282617.1:c.338A>T NP_001269546.1:p.Gln113Leu
NM_001282618.1:c.251A>T NP_001269547.1:p.Gln84Leu
NM_001282619.1:c.446A>T NP_001269548.1:p.Gln149Leu
NM_001282620.1:c.446A>T NP_001269549.1:p.Gln149Leu
NM_002070.3:c.494A>T NP_002061.1:p.Gln165Leu
NM_002070.4:c.494A>T MANE Select NP_002061.1:p.Gln165Leu
NM_001166425.2:c.383A>T NP_001159897.1:p.Gln128Leu
NM_001282618.2:c.251A>T NP_001269547.1:p.Gln84Leu
NM_001282619.2:c.446A>T NP_001269548.1:p.Gln149Leu
NM_001282620.2:c.446A>T NP_001269549.1:p.Gln149Leu
NM_001282617.2:c.338A>T NP_001269546.1:p.Gln113Leu