Canonical Allele Identifier: CA433695370

Gene: GNAI2

Linked Data

• MyVariant Identifiers: chr3:g.50293699A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256267A>G , CM000665.2:g.50256267A>G	GRCh38
NC_000003.11:g.50293699A>G , CM000665.1:g.50293699A>G	GRCh37
NC_000003.10:g.50268703A>G	NCBI36
NG_016002.2:g.34580A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000313601.11:c.540A>G MANE Select	ENSP00000312999.6:p.Val180=
ENST00000266027.9:c.384A>G	ENSP00000266027.6:p.Val128=
ENST00000313601.10:c.540A>G	ENSP00000312999.6:p.Val180=
ENST00000422163.5:c.492A>G	ENSP00000406871.1:p.Val164=
ENST00000440628.5:c.384A>G	ENSP00000395736.1:p.Val128=
ENST00000441156.5:c.*68A>G	ENSP00000394321.1:n.*68A>G
ENST00000446079.5:c.*175A>G	ENSP00000406065.1:n.*175A>G
ENST00000451956.1:c.429A>G	ENSP00000406369.1:p.Val143=
ENST00000468422.1:n.107A>G
ENST00000490122.5:n.1367A>G
ENST00000491100.5:n.2356A>G
NM_001166425.1:c.429A>G	NP_001159897.1:p.Val143=
NM_001282617.1:c.384A>G	NP_001269546.1:p.Val128=
NM_001282618.1:c.297A>G	NP_001269547.1:p.Val99=
NM_001282619.1:c.492A>G	NP_001269548.1:p.Val164=
NM_001282620.1:c.492A>G	NP_001269549.1:p.Val164=
NM_002070.3:c.540A>G	NP_002061.1:p.Val180=
NM_002070.4:c.540A>G MANE Select	NP_002061.1:p.Val180=
NM_001166425.2:c.429A>G	NP_001159897.1:p.Val143=
NM_001282618.2:c.297A>G	NP_001269547.1:p.Val99=
NM_001282619.2:c.492A>G	NP_001269548.1:p.Val164=
NM_001282620.2:c.492A>G	NP_001269549.1:p.Val164=
NM_001282617.2:c.384A>G	NP_001269546.1:p.Val128=