Canonical Allele Identifier: CA1363865460

Gene: GNAI2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256201C= , CM000665.2:g.50256201C=	GRCh38
NC_000003.11:g.50293633C= , CM000665.1:g.50293633C=	GRCh37
NC_000003.10:g.50268637C=	NCBI36
NG_016002.2:g.34514C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.474C= MANE Select	ENSP00000312999.6:p.Asn158=
ENST00000266027.9:c.318C=	ENSP00000266027.6:p.Asn106=
ENST00000313601.10:c.474C=	ENSP00000312999.6:p.Asn158=
ENST00000422163.5:c.426C=	ENSP00000406871.1:p.Asn142=
ENST00000440628.5:c.318C=	ENSP00000395736.1:p.Asn106=
ENST00000441156.5:c.*2C=	ENSP00000394321.1:n.*2C=
ENST00000446079.5:c.*109C=	ENSP00000406065.1:n.*109C=
ENST00000451956.1:c.363C=	ENSP00000406369.1:p.Asn121=
ENST00000468422.1:n.41C=
ENST00000490122.5:n.1301C=
ENST00000491100.5:n.2290C=
NM_001166425.1:c.363C=	NP_001159897.1:p.Asn121=
NM_001282617.1:c.318C=	NP_001269546.1:p.Asn106=
NM_001282618.1:c.231C=	NP_001269547.1:p.Asn77=
NM_001282619.1:c.426C=	NP_001269548.1:p.Asn142=
NM_001282620.1:c.426C=	NP_001269549.1:p.Asn142=
NM_002070.3:c.474C=	NP_002061.1:p.Asn158=
NM_002070.4:c.474C= MANE Select	NP_002061.1:p.Asn158=
NM_001166425.2:c.363C=	NP_001159897.1:p.Asn121=
NM_001282618.2:c.231C=	NP_001269547.1:p.Asn77=
NM_001282619.2:c.426C=	NP_001269548.1:p.Asn142=
NM_001282620.2:c.426C=	NP_001269549.1:p.Asn142=
NM_001282617.2:c.318C=	NP_001269546.1:p.Asn106=