Canonical Allele Identifier: CA433695412

Gene: GNAI2

Linked Data

• MyVariant Identifiers: chr3:g.50293708G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256276G>T , CM000665.2:g.50256276G>T	GRCh38
NC_000003.11:g.50293708G>T , CM000665.1:g.50293708G>T	GRCh37
NC_000003.10:g.50268712G>T	NCBI36
NG_016002.2:g.34589G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.549G>T MANE Select	ENSP00000312999.6:p.Thr183=
ENST00000266027.9:c.393G>T	ENSP00000266027.6:p.Thr131=
ENST00000313601.10:c.549G>T	ENSP00000312999.6:p.Thr183=
ENST00000422163.5:c.501G>T	ENSP00000406871.1:p.Thr167=
ENST00000440628.5:c.393G>T	ENSP00000395736.1:p.Thr131=
ENST00000441156.5:c.*77G>T	ENSP00000394321.1:n.*77G>T
ENST00000446079.5:c.*184G>T	ENSP00000406065.1:n.*184G>T
ENST00000451956.1:c.438G>T	ENSP00000406369.1:p.Thr146=
ENST00000468422.1:n.116G>T
ENST00000490122.5:n.1376G>T
ENST00000491100.5:n.2365G>T
NM_001166425.1:c.438G>T	NP_001159897.1:p.Thr146=
NM_001282617.1:c.393G>T	NP_001269546.1:p.Thr131=
NM_001282618.1:c.306G>T	NP_001269547.1:p.Thr102=
NM_001282619.1:c.501G>T	NP_001269548.1:p.Thr167=
NM_001282620.1:c.501G>T	NP_001269549.1:p.Thr167=
NM_002070.3:c.549G>T	NP_002061.1:p.Thr183=
NM_002070.4:c.549G>T MANE Select	NP_002061.1:p.Thr183=
NM_001166425.2:c.438G>T	NP_001159897.1:p.Thr146=
NM_001282618.2:c.306G>T	NP_001269547.1:p.Thr102=
NM_001282619.2:c.501G>T	NP_001269548.1:p.Thr167=
NM_001282620.2:c.501G>T	NP_001269549.1:p.Thr167=
NM_001282617.2:c.393G>T	NP_001269546.1:p.Thr131=