Canonical Allele Identifier: CA1363865452

Gene: GNAI2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256197T= , CM000665.2:g.50256197T=	GRCh38
NC_000003.11:g.50293629T= , CM000665.1:g.50293629T=	GRCh37
NC_000003.10:g.50268633T=	NCBI36
NG_016002.2:g.34510T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.470T= MANE Select	ENSP00000312999.6:p.Leu157=
ENST00000266027.9:c.314T=	ENSP00000266027.6:p.Leu105=
ENST00000313601.10:c.470T=	ENSP00000312999.6:p.Leu157=
ENST00000422163.5:c.422T=	ENSP00000406871.1:p.Leu141=
ENST00000440628.5:c.314T=	ENSP00000395736.1:p.Leu105=
ENST00000441156.5:c.427T=	ENSP00000394321.1:p.Ter143=
ENST00000446079.5:c.*105T=	ENSP00000406065.1:n.*105T=
ENST00000451956.1:c.359T=	ENSP00000406369.1:p.Leu120=
ENST00000468422.1:n.37T=
ENST00000490122.5:n.1297T=
ENST00000491100.5:n.2286T=
NM_001166425.1:c.359T=	NP_001159897.1:p.Leu120=
NM_001282617.1:c.314T=	NP_001269546.1:p.Leu105=
NM_001282618.1:c.227T=	NP_001269547.1:p.Leu76=
NM_001282619.1:c.422T=	NP_001269548.1:p.Leu141=
NM_001282620.1:c.422T=	NP_001269549.1:p.Leu141=
NM_002070.3:c.470T=	NP_002061.1:p.Leu157=
NM_002070.4:c.470T= MANE Select	NP_002061.1:p.Leu157=
NM_001166425.2:c.359T=	NP_001159897.1:p.Leu120=
NM_001282618.2:c.227T=	NP_001269547.1:p.Leu76=
NM_001282619.2:c.422T=	NP_001269548.1:p.Leu141=
NM_001282620.2:c.422T=	NP_001269549.1:p.Leu141=
NM_001282617.2:c.314T=	NP_001269546.1:p.Leu105=