Canonical Allele Identifier: CA1363859421

Gene: GNAI2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50243681T= , CM000665.2:g.50243681T=	GRCh38
NC_000003.11:g.50281113T= , CM000665.1:g.50281113T=	GRCh37
NC_000003.10:g.50256117T=	NCBI36
NG_016002.2:g.21994T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.118+7228T= MANE Select	ENSP00000312999.6:n.118+7228T=
ENST00000266027.9:c.-38-8419T=	ENSP00000266027.6:n.-38-8419T=
ENST00000313601.10:c.118+7228T=	ENSP00000312999.6:n.118+7228T=
ENST00000422163.5:c.71-8419T=	ENSP00000406871.1:n.71-8419T=
ENST00000440628.5:c.-39+5265T=	ENSP00000395736.1:n.-39+5265T=
ENST00000441156.5:c.118+7228T=	ENSP00000394321.1:n.118+7228T=
ENST00000446079.5:c.71-7939T=	ENSP00000406065.1:n.71-7939T=
ENST00000491100.5:n.1935-8419T=
NM_001282617.1:c.-38-8419T=	NP_001269546.1:n.-38-8419T=
NM_001282618.1:c.-83+7228T=	NP_001269547.1:n.-83+7228T=
NM_001282619.1:c.-54-7939T=	NP_001269548.1:n.-54-7939T=
NM_001282620.1:c.71-8419T=	NP_001269549.1:n.71-8419T=
NM_002070.3:c.118+7228T=	NP_002061.1:n.118+7228T=
NM_002070.4:c.118+7228T= MANE Select	NP_002061.1:n.118+7228T=
NM_001282618.2:c.-83+7228T=	NP_001269547.1:n.-83+7228T=
NM_001282619.2:c.-54-7939T=	NP_001269548.1:n.-54-7939T=
NM_001282620.2:c.71-8419T=	NP_001269549.1:n.71-8419T=
NM_001282617.2:c.-38-8419T=	NP_001269546.1:n.-38-8419T=