Canonical Allele Identifier: CA1363865476

Gene: GNAI2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256217G= , CM000665.2:g.50256217G=	GRCh38
NC_000003.11:g.50293649G= , CM000665.1:g.50293649G=	GRCh37
NC_000003.10:g.50268653G=	NCBI36
NG_016002.2:g.34530G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.490G= MANE Select	ENSP00000312999.6:p.Ala164=
ENST00000266027.9:c.334G=	ENSP00000266027.6:p.Ala112=
ENST00000313601.10:c.490G=	ENSP00000312999.6:p.Ala164=
ENST00000422163.5:c.442G=	ENSP00000406871.1:p.Ala148=
ENST00000440628.5:c.334G=	ENSP00000395736.1:p.Ala112=
ENST00000441156.5:c.*18G=	ENSP00000394321.1:n.*18G=
ENST00000446079.5:c.*125G=	ENSP00000406065.1:n.*125G=
ENST00000451956.1:c.379G=	ENSP00000406369.1:p.Ala127=
ENST00000468422.1:n.57G=
ENST00000490122.5:n.1317G=
ENST00000491100.5:n.2306G=
NM_001166425.1:c.379G=	NP_001159897.1:p.Ala127=
NM_001282617.1:c.334G=	NP_001269546.1:p.Ala112=
NM_001282618.1:c.247G=	NP_001269547.1:p.Ala83=
NM_001282619.1:c.442G=	NP_001269548.1:p.Ala148=
NM_001282620.1:c.442G=	NP_001269549.1:p.Ala148=
NM_002070.3:c.490G=	NP_002061.1:p.Ala164=
NM_002070.4:c.490G= MANE Select	NP_002061.1:p.Ala164=
NM_001166425.2:c.379G=	NP_001159897.1:p.Ala127=
NM_001282618.2:c.247G=	NP_001269547.1:p.Ala83=
NM_001282619.2:c.442G=	NP_001269548.1:p.Ala148=
NM_001282620.2:c.442G=	NP_001269549.1:p.Ala148=
NM_001282617.2:c.334G=	NP_001269546.1:p.Ala112=