Canonical Allele Identifier: CA352895636

Gene: GNAI2

Linked Data

• MyVariant Identifiers: chr3:g.50293704C>A (hg19) ; chr3:g.50256272C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256272C>A , CM000665.2:g.50256272C>A	GRCh38
NC_000003.11:g.50293704C>A , CM000665.1:g.50293704C>A	GRCh37
NC_000003.10:g.50268708C>A	NCBI36
NG_016002.2:g.34585C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000313601.11:c.545C>A MANE Select	ENSP00000312999.6:p.Thr182Asn
ENST00000266027.9:c.389C>A	ENSP00000266027.6:p.Thr130Asn
ENST00000313601.10:c.545C>A	ENSP00000312999.6:p.Thr182Asn
ENST00000422163.5:c.497C>A	ENSP00000406871.1:p.Thr166Asn
ENST00000440628.5:c.389C>A	ENSP00000395736.1:p.Thr130Asn
ENST00000441156.5:c.*73C>A	ENSP00000394321.1:n.*73C>A
ENST00000446079.5:c.*180C>A	ENSP00000406065.1:n.*180C>A
ENST00000451956.1:c.434C>A	ENSP00000406369.1:p.Thr145Asn
ENST00000468422.1:n.112C>A
ENST00000490122.5:n.1372C>A
ENST00000491100.5:n.2361C>A
NM_001166425.1:c.434C>A	NP_001159897.1:p.Thr145Asn
NM_001282617.1:c.389C>A	NP_001269546.1:p.Thr130Asn
NM_001282618.1:c.302C>A	NP_001269547.1:p.Thr101Asn
NM_001282619.1:c.497C>A	NP_001269548.1:p.Thr166Asn
NM_001282620.1:c.497C>A	NP_001269549.1:p.Thr166Asn
NM_002070.3:c.545C>A	NP_002061.1:p.Thr182Asn
NM_002070.4:c.545C>A MANE Select	NP_002061.1:p.Thr182Asn
NM_001166425.2:c.434C>A	NP_001159897.1:p.Thr145Asn
NM_001282618.2:c.302C>A	NP_001269547.1:p.Thr101Asn
NM_001282619.2:c.497C>A	NP_001269548.1:p.Thr166Asn
NM_001282620.2:c.497C>A	NP_001269549.1:p.Thr166Asn
NM_001282617.2:c.389C>A	NP_001269546.1:p.Thr130Asn