Canonical Allele Identifier: CA352895429

Gene: GNAI2

Linked Data

• MyVariant Identifiers: chr3:g.50293679G>T (hg19) ; chr3:g.50256247G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256247G>T , CM000665.2:g.50256247G>T	GRCh38
NC_000003.11:g.50293679G>T , CM000665.1:g.50293679G>T	GRCh37
NC_000003.10:g.50268683G>T	NCBI36
NG_016002.2:g.34560G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.520G>T MANE Select	ENSP00000312999.6:p.Asp174Tyr
ENST00000266027.9:c.364G>T	ENSP00000266027.6:p.Asp122Tyr
ENST00000313601.10:c.520G>T	ENSP00000312999.6:p.Asp174Tyr
ENST00000422163.5:c.472G>T	ENSP00000406871.1:p.Asp158Tyr
ENST00000440628.5:c.364G>T	ENSP00000395736.1:p.Asp122Tyr
ENST00000441156.5:c.*48G>T	ENSP00000394321.1:n.*48G>T
ENST00000446079.5:c.*155G>T	ENSP00000406065.1:n.*155G>T
ENST00000451956.1:c.409G>T	ENSP00000406369.1:p.Asp137Tyr
ENST00000468422.1:n.87G>T
ENST00000490122.5:n.1347G>T
ENST00000491100.5:n.2336G>T
NM_001166425.1:c.409G>T	NP_001159897.1:p.Asp137Tyr
NM_001282617.1:c.364G>T	NP_001269546.1:p.Asp122Tyr
NM_001282618.1:c.277G>T	NP_001269547.1:p.Asp93Tyr
NM_001282619.1:c.472G>T	NP_001269548.1:p.Asp158Tyr
NM_001282620.1:c.472G>T	NP_001269549.1:p.Asp158Tyr
NM_002070.3:c.520G>T	NP_002061.1:p.Asp174Tyr
NM_002070.4:c.520G>T MANE Select	NP_002061.1:p.Asp174Tyr
NM_001166425.2:c.409G>T	NP_001159897.1:p.Asp137Tyr
NM_001282618.2:c.277G>T	NP_001269547.1:p.Asp93Tyr
NM_001282619.2:c.472G>T	NP_001269548.1:p.Asp158Tyr
NM_001282620.2:c.472G>T	NP_001269549.1:p.Asp158Tyr
NM_001282617.2:c.364G>T	NP_001269546.1:p.Asp122Tyr