Canonical Allele Identifier: CA433694668

Gene: GNAI2

Linked Data

• MyVariant Identifiers: chr3:g.50293639G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256207G>C , CM000665.2:g.50256207G>C	GRCh38
NC_000003.11:g.50293639G>C , CM000665.1:g.50293639G>C	GRCh37
NC_000003.10:g.50268643G>C	NCBI36
NG_016002.2:g.34520G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.480G>C MANE Select	ENSP00000312999.6:p.Leu160=
ENST00000266027.9:c.324G>C	ENSP00000266027.6:p.Leu108=
ENST00000313601.10:c.480G>C	ENSP00000312999.6:p.Leu160=
ENST00000422163.5:c.432G>C	ENSP00000406871.1:p.Leu144=
ENST00000440628.5:c.324G>C	ENSP00000395736.1:p.Leu108=
ENST00000441156.5:c.*8G>C	ENSP00000394321.1:n.*8G>C
ENST00000446079.5:c.*115G>C	ENSP00000406065.1:n.*115G>C
ENST00000451956.1:c.369G>C	ENSP00000406369.1:p.Leu123=
ENST00000468422.1:n.47G>C
ENST00000490122.5:n.1307G>C
ENST00000491100.5:n.2296G>C
NM_001166425.1:c.369G>C	NP_001159897.1:p.Leu123=
NM_001282617.1:c.324G>C	NP_001269546.1:p.Leu108=
NM_001282618.1:c.237G>C	NP_001269547.1:p.Leu79=
NM_001282619.1:c.432G>C	NP_001269548.1:p.Leu144=
NM_001282620.1:c.432G>C	NP_001269549.1:p.Leu144=
NM_002070.3:c.480G>C	NP_002061.1:p.Leu160=
NM_002070.4:c.480G>C MANE Select	NP_002061.1:p.Leu160=
NM_001166425.2:c.369G>C	NP_001159897.1:p.Leu123=
NM_001282618.2:c.237G>C	NP_001269547.1:p.Leu79=
NM_001282619.2:c.432G>C	NP_001269548.1:p.Leu144=
NM_001282620.2:c.432G>C	NP_001269549.1:p.Leu144=
NM_001282617.2:c.324G>C	NP_001269546.1:p.Leu108=