Canonical Allele Identifier: CA352895143

Gene: GNAI2

Linked Data

• MyVariant Identifiers: chr3:g.50293656G>T (hg19) ; chr3:g.50256224G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256224G>T , CM000665.2:g.50256224G>T	GRCh38
NC_000003.11:g.50293656G>T , CM000665.1:g.50293656G>T	GRCh37
NC_000003.10:g.50268660G>T	NCBI36
NG_016002.2:g.34537G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.497G>T MANE Select	ENSP00000312999.6:p.Ser166Ile
ENST00000266027.9:c.341G>T	ENSP00000266027.6:p.Ser114Ile
ENST00000313601.10:c.497G>T	ENSP00000312999.6:p.Ser166Ile
ENST00000422163.5:c.449G>T	ENSP00000406871.1:p.Ser150Ile
ENST00000440628.5:c.341G>T	ENSP00000395736.1:p.Ser114Ile
ENST00000441156.5:c.*25G>T	ENSP00000394321.1:n.*25G>T
ENST00000446079.5:c.*132G>T	ENSP00000406065.1:n.*132G>T
ENST00000451956.1:c.386G>T	ENSP00000406369.1:p.Ser129Ile
ENST00000468422.1:n.64G>T
ENST00000490122.5:n.1324G>T
ENST00000491100.5:n.2313G>T
NM_001166425.1:c.386G>T	NP_001159897.1:p.Ser129Ile
NM_001282617.1:c.341G>T	NP_001269546.1:p.Ser114Ile
NM_001282618.1:c.254G>T	NP_001269547.1:p.Ser85Ile
NM_001282619.1:c.449G>T	NP_001269548.1:p.Ser150Ile
NM_001282620.1:c.449G>T	NP_001269549.1:p.Ser150Ile
NM_002070.3:c.497G>T	NP_002061.1:p.Ser166Ile
NM_002070.4:c.497G>T MANE Select	NP_002061.1:p.Ser166Ile
NM_001166425.2:c.386G>T	NP_001159897.1:p.Ser129Ile
NM_001282618.2:c.254G>T	NP_001269547.1:p.Ser85Ile
NM_001282619.2:c.449G>T	NP_001269548.1:p.Ser150Ile
NM_001282620.2:c.449G>T	NP_001269549.1:p.Ser150Ile
NM_001282617.2:c.341G>T	NP_001269546.1:p.Ser114Ile