Canonical Allele Identifier: CA352895336
Gene: GNAI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50256242A>C , CM000665.2:g.50256242A>C GRCh38
NC_000003.11:g.50293674A>C , CM000665.1:g.50293674A>C GRCh37
NC_000003.10:g.50268678A>C NCBI36
NG_016002.2:g.34555A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000313601.11:c.515A>C MANE Select ENSP00000312999.6:p.Gln172Pro
ENST00000266027.9:c.359A>C ENSP00000266027.6:p.Gln120Pro
ENST00000313601.10:c.515A>C ENSP00000312999.6:p.Gln172Pro
ENST00000422163.5:c.467A>C ENSP00000406871.1:p.Gln156Pro
ENST00000440628.5:c.359A>C ENSP00000395736.1:p.Gln120Pro
ENST00000441156.5:c.*43A>C ENSP00000394321.1:n.*43A>C
ENST00000446079.5:c.*150A>C ENSP00000406065.1:n.*150A>C
ENST00000451956.1:c.404A>C ENSP00000406369.1:p.Gln135Pro
ENST00000468422.1:n.82A>C
ENST00000490122.5:n.1342A>C
ENST00000491100.5:n.2331A>C
NM_001166425.1:c.404A>C NP_001159897.1:p.Gln135Pro
NM_001282617.1:c.359A>C NP_001269546.1:p.Gln120Pro
NM_001282618.1:c.272A>C NP_001269547.1:p.Gln91Pro
NM_001282619.1:c.467A>C NP_001269548.1:p.Gln156Pro
NM_001282620.1:c.467A>C NP_001269549.1:p.Gln156Pro
NM_002070.3:c.515A>C NP_002061.1:p.Gln172Pro
NM_002070.4:c.515A>C MANE Select NP_002061.1:p.Gln172Pro
NM_001166425.2:c.404A>C NP_001159897.1:p.Gln135Pro
NM_001282618.2:c.272A>C NP_001269547.1:p.Gln91Pro
NM_001282619.2:c.467A>C NP_001269548.1:p.Gln156Pro
NM_001282620.2:c.467A>C NP_001269549.1:p.Gln156Pro
NM_001282617.2:c.359A>C NP_001269546.1:p.Gln120Pro