Canonical Allele Identifier: CA1363865519

Gene: GNAI2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256282C= , CM000665.2:g.50256282C=	GRCh38
NC_000003.11:g.50293714C= , CM000665.1:g.50293714C=	GRCh37
NC_000003.10:g.50268718C=	NCBI36
NG_016002.2:g.34595C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.555C= MANE Select	ENSP00000312999.6:p.Ile185=
ENST00000266027.9:c.399C=	ENSP00000266027.6:p.Ile133=
ENST00000313601.10:c.555C=	ENSP00000312999.6:p.Ile185=
ENST00000422163.5:c.507C=	ENSP00000406871.1:p.Ile169=
ENST00000440628.5:c.399C=	ENSP00000395736.1:p.Ile133=
ENST00000441156.5:c.*83C=	ENSP00000394321.1:n.*83C=
ENST00000446079.5:c.*190C=	ENSP00000406065.1:n.*190C=
ENST00000451956.1:c.444C=	ENSP00000406369.1:p.Ile148=
ENST00000468422.1:n.122C=
ENST00000490122.5:n.1382C=
ENST00000491100.5:n.2371C=
NM_001166425.1:c.444C=	NP_001159897.1:p.Ile148=
NM_001282617.1:c.399C=	NP_001269546.1:p.Ile133=
NM_001282618.1:c.312C=	NP_001269547.1:p.Ile104=
NM_001282619.1:c.507C=	NP_001269548.1:p.Ile169=
NM_001282620.1:c.507C=	NP_001269549.1:p.Ile169=
NM_002070.3:c.555C=	NP_002061.1:p.Ile185=
NM_002070.4:c.555C= MANE Select	NP_002061.1:p.Ile185=
NM_001166425.2:c.444C=	NP_001159897.1:p.Ile148=
NM_001282618.2:c.312C=	NP_001269547.1:p.Ile104=
NM_001282619.2:c.507C=	NP_001269548.1:p.Ile169=
NM_001282620.2:c.507C=	NP_001269549.1:p.Ile169=
NM_001282617.2:c.399C=	NP_001269546.1:p.Ile133=