Canonical Allele Identifier: CA352895267

Gene: GNAI2

Linked Data

• MyVariant Identifiers: chr3:g.50293665T>G (hg19) ; chr3:g.50256233T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256233T>G , CM000665.2:g.50256233T>G	GRCh38
NC_000003.11:g.50293665T>G , CM000665.1:g.50293665T>G	GRCh37
NC_000003.10:g.50268669T>G	NCBI36
NG_016002.2:g.34546T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.506T>G MANE Select	ENSP00000312999.6:p.Ile169Ser
ENST00000266027.9:c.350T>G	ENSP00000266027.6:p.Ile117Ser
ENST00000313601.10:c.506T>G	ENSP00000312999.6:p.Ile169Ser
ENST00000422163.5:c.458T>G	ENSP00000406871.1:p.Ile153Ser
ENST00000440628.5:c.350T>G	ENSP00000395736.1:p.Ile117Ser
ENST00000441156.5:c.*34T>G	ENSP00000394321.1:n.*34T>G
ENST00000446079.5:c.*141T>G	ENSP00000406065.1:n.*141T>G
ENST00000451956.1:c.395T>G	ENSP00000406369.1:p.Ile132Ser
ENST00000468422.1:n.73T>G
ENST00000490122.5:n.1333T>G
ENST00000491100.5:n.2322T>G
NM_001166425.1:c.395T>G	NP_001159897.1:p.Ile132Ser
NM_001282617.1:c.350T>G	NP_001269546.1:p.Ile117Ser
NM_001282618.1:c.263T>G	NP_001269547.1:p.Ile88Ser
NM_001282619.1:c.458T>G	NP_001269548.1:p.Ile153Ser
NM_001282620.1:c.458T>G	NP_001269549.1:p.Ile153Ser
NM_002070.3:c.506T>G	NP_002061.1:p.Ile169Ser
NM_002070.4:c.506T>G MANE Select	NP_002061.1:p.Ile169Ser
NM_001166425.2:c.395T>G	NP_001159897.1:p.Ile132Ser
NM_001282618.2:c.263T>G	NP_001269547.1:p.Ile88Ser
NM_001282619.2:c.458T>G	NP_001269548.1:p.Ile153Ser
NM_001282620.2:c.458T>G	NP_001269549.1:p.Ile153Ser
NM_001282617.2:c.350T>G	NP_001269546.1:p.Ile117Ser