Canonical Allele Identifier: CA1363865449

Gene: GNAI2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256195C= , CM000665.2:g.50256195C=	GRCh38
NC_000003.11:g.50293627C= , CM000665.1:g.50293627C=	GRCh37
NC_000003.10:g.50268631C=	NCBI36
NG_016002.2:g.34508C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.468C= MANE Select	ENSP00000312999.6:p.Tyr156=
ENST00000266027.9:c.312C=	ENSP00000266027.6:p.Tyr104=
ENST00000313601.10:c.468C=	ENSP00000312999.6:p.Tyr156=
ENST00000422163.5:c.420C=	ENSP00000406871.1:p.Tyr140=
ENST00000440628.5:c.312C=	ENSP00000395736.1:p.Tyr104=
ENST00000441156.5:c.425C=	ENSP00000394321.1:p.Thr142=
ENST00000446079.5:c.*103C=	ENSP00000406065.1:n.*103C=
ENST00000451956.1:c.357C=	ENSP00000406369.1:p.Tyr119=
ENST00000468422.1:n.35C=
ENST00000490122.5:n.1295C=
ENST00000491100.5:n.2284C=
NM_001166425.1:c.357C=	NP_001159897.1:p.Tyr119=
NM_001282617.1:c.312C=	NP_001269546.1:p.Tyr104=
NM_001282618.1:c.225C=	NP_001269547.1:p.Tyr75=
NM_001282619.1:c.420C=	NP_001269548.1:p.Tyr140=
NM_001282620.1:c.420C=	NP_001269549.1:p.Tyr140=
NM_002070.3:c.468C=	NP_002061.1:p.Tyr156=
NM_002070.4:c.468C= MANE Select	NP_002061.1:p.Tyr156=
NM_001166425.2:c.357C=	NP_001159897.1:p.Tyr119=
NM_001282618.2:c.225C=	NP_001269547.1:p.Tyr75=
NM_001282619.2:c.420C=	NP_001269548.1:p.Tyr140=
NM_001282620.2:c.420C=	NP_001269549.1:p.Tyr140=
NM_001282617.2:c.312C=	NP_001269546.1:p.Tyr104=