Canonical Allele Identifier: CA352895297

Gene: GNAI2

Linked Data

• MyVariant Identifiers: chr3:g.50293667C>T (hg19) ; chr3:g.50256235C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256235C>T , CM000665.2:g.50256235C>T	GRCh38
NC_000003.11:g.50293667C>T , CM000665.1:g.50293667C>T	GRCh37
NC_000003.10:g.50268671C>T	NCBI36
NG_016002.2:g.34548C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.508C>T MANE Select	ENSP00000312999.6:p.Pro170Ser
ENST00000266027.9:c.352C>T	ENSP00000266027.6:p.Pro118Ser
ENST00000313601.10:c.508C>T	ENSP00000312999.6:p.Pro170Ser
ENST00000422163.5:c.460C>T	ENSP00000406871.1:p.Pro154Ser
ENST00000440628.5:c.352C>T	ENSP00000395736.1:p.Pro118Ser
ENST00000441156.5:c.*36C>T	ENSP00000394321.1:n.*36C>T
ENST00000446079.5:c.*143C>T	ENSP00000406065.1:n.*143C>T
ENST00000451956.1:c.397C>T	ENSP00000406369.1:p.Pro133Ser
ENST00000468422.1:n.75C>T
ENST00000490122.5:n.1335C>T
ENST00000491100.5:n.2324C>T
NM_001166425.1:c.397C>T	NP_001159897.1:p.Pro133Ser
NM_001282617.1:c.352C>T	NP_001269546.1:p.Pro118Ser
NM_001282618.1:c.265C>T	NP_001269547.1:p.Pro89Ser
NM_001282619.1:c.460C>T	NP_001269548.1:p.Pro154Ser
NM_001282620.1:c.460C>T	NP_001269549.1:p.Pro154Ser
NM_002070.3:c.508C>T	NP_002061.1:p.Pro170Ser
NM_002070.4:c.508C>T MANE Select	NP_002061.1:p.Pro170Ser
NM_001166425.2:c.397C>T	NP_001159897.1:p.Pro133Ser
NM_001282618.2:c.265C>T	NP_001269547.1:p.Pro89Ser
NM_001282619.2:c.460C>T	NP_001269548.1:p.Pro154Ser
NM_001282620.2:c.460C>T	NP_001269549.1:p.Pro154Ser
NM_001282617.2:c.352C>T	NP_001269546.1:p.Pro118Ser