Canonical Allele Identifier: CA352894880

Gene: GNAI2

Linked Data

• MyVariant Identifiers: chr3:g.50293637C>G (hg19) ; chr3:g.50256205C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256205C>G , CM000665.2:g.50256205C>G	GRCh38
NC_000003.11:g.50293637C>G , CM000665.1:g.50293637C>G	GRCh37
NC_000003.10:g.50268641C>G	NCBI36
NG_016002.2:g.34518C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.478C>G MANE Select	ENSP00000312999.6:p.Leu160Val
ENST00000266027.9:c.322C>G	ENSP00000266027.6:p.Leu108Val
ENST00000313601.10:c.478C>G	ENSP00000312999.6:p.Leu160Val
ENST00000422163.5:c.430C>G	ENSP00000406871.1:p.Leu144Val
ENST00000440628.5:c.322C>G	ENSP00000395736.1:p.Leu108Val
ENST00000441156.5:c.*6C>G	ENSP00000394321.1:n.*6C>G
ENST00000446079.5:c.*113C>G	ENSP00000406065.1:n.*113C>G
ENST00000451956.1:c.367C>G	ENSP00000406369.1:p.Leu123Val
ENST00000468422.1:n.45C>G
ENST00000490122.5:n.1305C>G
ENST00000491100.5:n.2294C>G
NM_001166425.1:c.367C>G	NP_001159897.1:p.Leu123Val
NM_001282617.1:c.322C>G	NP_001269546.1:p.Leu108Val
NM_001282618.1:c.235C>G	NP_001269547.1:p.Leu79Val
NM_001282619.1:c.430C>G	NP_001269548.1:p.Leu144Val
NM_001282620.1:c.430C>G	NP_001269549.1:p.Leu144Val
NM_002070.3:c.478C>G	NP_002061.1:p.Leu160Val
NM_002070.4:c.478C>G MANE Select	NP_002061.1:p.Leu160Val
NM_001166425.2:c.367C>G	NP_001159897.1:p.Leu123Val
NM_001282618.2:c.235C>G	NP_001269547.1:p.Leu79Val
NM_001282619.2:c.430C>G	NP_001269548.1:p.Leu144Val
NM_001282620.2:c.430C>G	NP_001269549.1:p.Leu144Val
NM_001282617.2:c.322C>G	NP_001269546.1:p.Leu108Val