Canonical Allele Identifier: CA1363865504

Gene: GNAI2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256262C= , CM000665.2:g.50256262C=	GRCh38
NC_000003.11:g.50293694C= , CM000665.1:g.50293694C=	GRCh37
NC_000003.10:g.50268698C=	NCBI36
NG_016002.2:g.34575C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.535C= MANE Select	ENSP00000312999.6:p.Arg179=
ENST00000266027.9:c.379C=	ENSP00000266027.6:p.Arg127=
ENST00000313601.10:c.535C=	ENSP00000312999.6:p.Arg179=
ENST00000422163.5:c.487C=	ENSP00000406871.1:p.Arg163=
ENST00000440628.5:c.379C=	ENSP00000395736.1:p.Arg127=
ENST00000441156.5:c.*63C=	ENSP00000394321.1:n.*63C=
ENST00000446079.5:c.*170C=	ENSP00000406065.1:n.*170C=
ENST00000451956.1:c.424C=	ENSP00000406369.1:p.Arg142=
ENST00000468422.1:n.102C=
ENST00000490122.5:n.1362C=
ENST00000491100.5:n.2351C=
NM_001166425.1:c.424C=	NP_001159897.1:p.Arg142=
NM_001282617.1:c.379C=	NP_001269546.1:p.Arg127=
NM_001282618.1:c.292C=	NP_001269547.1:p.Arg98=
NM_001282619.1:c.487C=	NP_001269548.1:p.Arg163=
NM_001282620.1:c.487C=	NP_001269549.1:p.Arg163=
NM_002070.3:c.535C=	NP_002061.1:p.Arg179=
NM_002070.4:c.535C= MANE Select	NP_002061.1:p.Arg179=
NM_001166425.2:c.424C=	NP_001159897.1:p.Arg142=
NM_001282618.2:c.292C=	NP_001269547.1:p.Arg98=
NM_001282619.2:c.487C=	NP_001269548.1:p.Arg163=
NM_001282620.2:c.487C=	NP_001269549.1:p.Arg163=
NM_001282617.2:c.379C=	NP_001269546.1:p.Arg127=