Canonical Allele Identifier: CA352895579

Gene: GNAI2

Linked Data

• MyVariant Identifiers: chr3:g.50293697G>C (hg19) ; chr3:g.50256265G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256265G>C , CM000665.2:g.50256265G>C	GRCh38
NC_000003.11:g.50293697G>C , CM000665.1:g.50293697G>C	GRCh37
NC_000003.10:g.50268701G>C	NCBI36
NG_016002.2:g.34578G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.538G>C MANE Select	ENSP00000312999.6:p.Val180Leu
ENST00000266027.9:c.382G>C	ENSP00000266027.6:p.Val128Leu
ENST00000313601.10:c.538G>C	ENSP00000312999.6:p.Val180Leu
ENST00000422163.5:c.490G>C	ENSP00000406871.1:p.Val164Leu
ENST00000440628.5:c.382G>C	ENSP00000395736.1:p.Val128Leu
ENST00000441156.5:c.*66G>C	ENSP00000394321.1:n.*66G>C
ENST00000446079.5:c.*173G>C	ENSP00000406065.1:n.*173G>C
ENST00000451956.1:c.427G>C	ENSP00000406369.1:p.Val143Leu
ENST00000468422.1:n.105G>C
ENST00000490122.5:n.1365G>C
ENST00000491100.5:n.2354G>C
NM_001166425.1:c.427G>C	NP_001159897.1:p.Val143Leu
NM_001282617.1:c.382G>C	NP_001269546.1:p.Val128Leu
NM_001282618.1:c.295G>C	NP_001269547.1:p.Val99Leu
NM_001282619.1:c.490G>C	NP_001269548.1:p.Val164Leu
NM_001282620.1:c.490G>C	NP_001269549.1:p.Val164Leu
NM_002070.3:c.538G>C	NP_002061.1:p.Val180Leu
NM_002070.4:c.538G>C MANE Select	NP_002061.1:p.Val180Leu
NM_001166425.2:c.427G>C	NP_001159897.1:p.Val143Leu
NM_001282618.2:c.295G>C	NP_001269547.1:p.Val99Leu
NM_001282619.2:c.490G>C	NP_001269548.1:p.Val164Leu
NM_001282620.2:c.490G>C	NP_001269549.1:p.Val164Leu
NM_001282617.2:c.382G>C	NP_001269546.1:p.Val128Leu