Canonical Allele Identifier: CA1363865389

Gene: GNAI2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256176C= , CM000665.2:g.50256176C=	GRCh38
NC_000003.11:g.50293608C= , CM000665.1:g.50293608C=	GRCh37
NC_000003.10:g.50268612C=	NCBI36
NG_016002.2:g.34489C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.465-16C= MANE Select	ENSP00000312999.6:n.465-16C=
ENST00000266027.9:c.309-16C=	ENSP00000266027.6:n.309-16C=
ENST00000313601.10:c.465-16C=	ENSP00000312999.6:n.465-16C=
ENST00000422163.5:c.417-16C=	ENSP00000406871.1:n.417-16C=
ENST00000440628.5:c.309-16C=	ENSP00000395736.1:n.309-16C=
ENST00000441156.5:c.422-16C=	ENSP00000394321.1:n.422-16C=
ENST00000446079.5:c.*100-16C=	ENSP00000406065.1:n.*100-16C=
ENST00000451956.1:c.354-16C=	ENSP00000406369.1:n.354-16C=
ENST00000468422.1:n.32-16C=
ENST00000490122.5:n.1292-16C=
ENST00000491100.5:n.2281-16C=
NM_001166425.1:c.354-16C=	NP_001159897.1:n.354-16C=
NM_001282617.1:c.309-16C=	NP_001269546.1:n.309-16C=
NM_001282618.1:c.222-16C=	NP_001269547.1:n.222-16C=
NM_001282619.1:c.417-16C=	NP_001269548.1:n.417-16C=
NM_001282620.1:c.417-16C=	NP_001269549.1:n.417-16C=
NM_002070.3:c.465-16C=	NP_002061.1:n.465-16C=
NM_002070.4:c.465-16C= MANE Select	NP_002061.1:n.465-16C=
NM_001166425.2:c.354-16C=	NP_001159897.1:n.354-16C=
NM_001282618.2:c.222-16C=	NP_001269547.1:n.222-16C=
NM_001282619.2:c.417-16C=	NP_001269548.1:n.417-16C=
NM_001282620.2:c.417-16C=	NP_001269549.1:n.417-16C=
NM_001282617.2:c.309-16C=	NP_001269546.1:n.309-16C=