Canonical Allele Identifier: CA1363865472

Gene: GNAI2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256210G= , CM000665.2:g.50256210G=	GRCh38
NC_000003.11:g.50293642G= , CM000665.1:g.50293642G=	GRCh37
NC_000003.10:g.50268646G=	NCBI36
NG_016002.2:g.34523G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.483G= MANE Select	ENSP00000312999.6:p.Glu161=
ENST00000266027.9:c.327G=	ENSP00000266027.6:p.Glu109=
ENST00000313601.10:c.483G=	ENSP00000312999.6:p.Glu161=
ENST00000422163.5:c.435G=	ENSP00000406871.1:p.Glu145=
ENST00000440628.5:c.327G=	ENSP00000395736.1:p.Glu109=
ENST00000441156.5:c.*11G=	ENSP00000394321.1:n.*11G=
ENST00000446079.5:c.*118G=	ENSP00000406065.1:n.*118G=
ENST00000451956.1:c.372G=	ENSP00000406369.1:p.Glu124=
ENST00000468422.1:n.50G=
ENST00000490122.5:n.1310G=
ENST00000491100.5:n.2299G=
NM_001166425.1:c.372G=	NP_001159897.1:p.Glu124=
NM_001282617.1:c.327G=	NP_001269546.1:p.Glu109=
NM_001282618.1:c.240G=	NP_001269547.1:p.Glu80=
NM_001282619.1:c.435G=	NP_001269548.1:p.Glu145=
NM_001282620.1:c.435G=	NP_001269549.1:p.Glu145=
NM_002070.3:c.483G=	NP_002061.1:p.Glu161=
NM_002070.4:c.483G= MANE Select	NP_002061.1:p.Glu161=
NM_001166425.2:c.372G=	NP_001159897.1:p.Glu124=
NM_001282618.2:c.240G=	NP_001269547.1:p.Glu80=
NM_001282619.2:c.435G=	NP_001269548.1:p.Glu145=
NM_001282620.2:c.435G=	NP_001269549.1:p.Glu145=
NM_001282617.2:c.327G=	NP_001269546.1:p.Glu109=