Canonical Allele Identifier: CA1363865446

Gene: GNAI2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256193T= , CM000665.2:g.50256193T=	GRCh38
NC_000003.11:g.50293625T= , CM000665.1:g.50293625T=	GRCh37
NC_000003.10:g.50268629T=	NCBI36
NG_016002.2:g.34506T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.466T= MANE Select	ENSP00000312999.6:p.Tyr156=
ENST00000266027.9:c.310T=	ENSP00000266027.6:p.Tyr104=
ENST00000313601.10:c.466T=	ENSP00000312999.6:p.Tyr156=
ENST00000422163.5:c.418T=	ENSP00000406871.1:p.Tyr140=
ENST00000440628.5:c.310T=	ENSP00000395736.1:p.Tyr104=
ENST00000441156.5:c.423T=	ENSP00000394321.1:p.Thr141=
ENST00000446079.5:c.*101T=	ENSP00000406065.1:n.*101T=
ENST00000451956.1:c.355T=	ENSP00000406369.1:p.Tyr119=
ENST00000468422.1:n.33T=
ENST00000490122.5:n.1293T=
ENST00000491100.5:n.2282T=
NM_001166425.1:c.355T=	NP_001159897.1:p.Tyr119=
NM_001282617.1:c.310T=	NP_001269546.1:p.Tyr104=
NM_001282618.1:c.223T=	NP_001269547.1:p.Tyr75=
NM_001282619.1:c.418T=	NP_001269548.1:p.Tyr140=
NM_001282620.1:c.418T=	NP_001269549.1:p.Tyr140=
NM_002070.3:c.466T=	NP_002061.1:p.Tyr156=
NM_002070.4:c.466T= MANE Select	NP_002061.1:p.Tyr156=
NM_001166425.2:c.355T=	NP_001159897.1:p.Tyr119=
NM_001282618.2:c.223T=	NP_001269547.1:p.Tyr75=
NM_001282619.2:c.418T=	NP_001269548.1:p.Tyr140=
NM_001282620.2:c.418T=	NP_001269549.1:p.Tyr140=
NM_001282617.2:c.310T=	NP_001269546.1:p.Tyr104=