Canonical Allele Identifier: CA1363865552

Gene: GNAI2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256335G= , CM000665.2:g.50256335G=	GRCh38
NC_000003.11:g.50293767G= , CM000665.1:g.50293767G=	GRCh37
NC_000003.10:g.50268771G=	NCBI36
NG_016002.2:g.34648G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.593+15G= MANE Select	ENSP00000312999.6:n.593+15G=
ENST00000266027.9:c.437+15G=	ENSP00000266027.6:n.437+15G=
ENST00000313601.10:c.593+15G=	ENSP00000312999.6:n.593+15G=
ENST00000422163.5:c.545+15G=	ENSP00000406871.1:n.545+15G=
ENST00000440628.5:c.437+15G=	ENSP00000395736.1:n.437+15G=
ENST00000441156.5:c.*121+15G=	ENSP00000394321.1:n.*121+15G=
ENST00000446079.5:c.*228+15G=	ENSP00000406065.1:n.*228+15G=
ENST00000451956.1:c.482+15G=	ENSP00000406369.1:n.482+15G=
ENST00000468422.1:n.175G=
ENST00000490122.5:n.1420+15G=
ENST00000491100.5:n.2409+15G=
ENST00000492383.1:n.38+15G=
NM_001166425.1:c.482+15G=	NP_001159897.1:n.482+15G=
NM_001282617.1:c.437+15G=	NP_001269546.1:n.437+15G=
NM_001282618.1:c.350+15G=	NP_001269547.1:n.350+15G=
NM_001282619.1:c.545+15G=	NP_001269548.1:n.545+15G=
NM_001282620.1:c.545+15G=	NP_001269549.1:n.545+15G=
NM_002070.3:c.593+15G=	NP_002061.1:n.593+15G=
NM_002070.4:c.593+15G= MANE Select	NP_002061.1:n.593+15G=
NM_001166425.2:c.482+15G=	NP_001159897.1:n.482+15G=
NM_001282618.2:c.350+15G=	NP_001269547.1:n.350+15G=
NM_001282619.2:c.545+15G=	NP_001269548.1:n.545+15G=
NM_001282620.2:c.545+15G=	NP_001269549.1:n.545+15G=
NM_001282617.2:c.437+15G=	NP_001269546.1:n.437+15G=