Canonical Allele Identifier: CA433694652

Gene: GNAI2

Linked Data

• COSMIC: COSM377926
• MyVariant Identifiers: chr3:g.50293636C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256204C>T , CM000665.2:g.50256204C>T	GRCh38
NC_000003.11:g.50293636C>T , CM000665.1:g.50293636C>T	GRCh37
NC_000003.10:g.50268640C>T	NCBI36
NG_016002.2:g.34517C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.477C>T MANE Select	ENSP00000312999.6:p.Asp159=
ENST00000266027.9:c.321C>T	ENSP00000266027.6:p.Asp107=
ENST00000313601.10:c.477C>T	ENSP00000312999.6:p.Asp159=
ENST00000422163.5:c.429C>T	ENSP00000406871.1:p.Asp143=
ENST00000440628.5:c.321C>T	ENSP00000395736.1:p.Asp107=
ENST00000441156.5:c.*5C>T	ENSP00000394321.1:n.*5C>T
ENST00000446079.5:c.*112C>T	ENSP00000406065.1:n.*112C>T
ENST00000451956.1:c.366C>T	ENSP00000406369.1:p.Asp122=
ENST00000468422.1:n.44C>T
ENST00000490122.5:n.1304C>T
ENST00000491100.5:n.2293C>T
NM_001166425.1:c.366C>T	NP_001159897.1:p.Asp122=
NM_001282617.1:c.321C>T	NP_001269546.1:p.Asp107=
NM_001282618.1:c.234C>T	NP_001269547.1:p.Asp78=
NM_001282619.1:c.429C>T	NP_001269548.1:p.Asp143=
NM_001282620.1:c.429C>T	NP_001269549.1:p.Asp143=
NM_002070.3:c.477C>T	NP_002061.1:p.Asp159=
NM_002070.4:c.477C>T MANE Select	NP_002061.1:p.Asp159=
NM_001166425.2:c.366C>T	NP_001159897.1:p.Asp122=
NM_001282618.2:c.234C>T	NP_001269547.1:p.Asp78=
NM_001282619.2:c.429C>T	NP_001269548.1:p.Asp143=
NM_001282620.2:c.429C>T	NP_001269549.1:p.Asp143=
NM_001282617.2:c.321C>T	NP_001269546.1:p.Asp107=