Canonical Allele Identifier: CA1363865488

Gene: GNAI2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256246A= , CM000665.2:g.50256246A=	GRCh38
NC_000003.11:g.50293678A= , CM000665.1:g.50293678A=	GRCh37
NC_000003.10:g.50268682A=	NCBI36
NG_016002.2:g.34559A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.519A= MANE Select	ENSP00000312999.6:p.Gln173=
ENST00000266027.9:c.363A=	ENSP00000266027.6:p.Gln121=
ENST00000313601.10:c.519A=	ENSP00000312999.6:p.Gln173=
ENST00000422163.5:c.471A=	ENSP00000406871.1:p.Gln157=
ENST00000440628.5:c.363A=	ENSP00000395736.1:p.Gln121=
ENST00000441156.5:c.*47A=	ENSP00000394321.1:n.*47A=
ENST00000446079.5:c.*154A=	ENSP00000406065.1:n.*154A=
ENST00000451956.1:c.408A=	ENSP00000406369.1:p.Gln136=
ENST00000468422.1:n.86A=
ENST00000490122.5:n.1346A=
ENST00000491100.5:n.2335A=
NM_001166425.1:c.408A=	NP_001159897.1:p.Gln136=
NM_001282617.1:c.363A=	NP_001269546.1:p.Gln121=
NM_001282618.1:c.276A=	NP_001269547.1:p.Gln92=
NM_001282619.1:c.471A=	NP_001269548.1:p.Gln157=
NM_001282620.1:c.471A=	NP_001269549.1:p.Gln157=
NM_002070.3:c.519A=	NP_002061.1:p.Gln173=
NM_002070.4:c.519A= MANE Select	NP_002061.1:p.Gln173=
NM_001166425.2:c.408A=	NP_001159897.1:p.Gln136=
NM_001282618.2:c.276A=	NP_001269547.1:p.Gln92=
NM_001282619.2:c.471A=	NP_001269548.1:p.Gln157=
NM_001282620.2:c.471A=	NP_001269549.1:p.Gln157=
NM_001282617.2:c.363A=	NP_001269546.1:p.Gln121=