Canonical Allele Identifier: CA371857414
Gene: OSR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98949356A>G , CM000670.2:g.98949356A>G GRCh38
NC_000008.10:g.99961584A>G , CM000670.1:g.99961584A>G GRCh37
NC_000008.9:g.100030760A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000297565.9:c.404A>G MANE Select ENSP00000297565.4:p.Asp135Gly
ENST00000297565.8:c.404A>G ENSP00000297565.4:p.Asp135Gly
ENST00000435298.6:c.404A>G ENSP00000402862.2:p.Asp135Gly
ENST00000457907.3:c.767A>G ENSP00000414657.2:p.Asp256Gly
ENST00000518199.1:c.404A>G ENSP00000429910.1:p.Asp135Gly
ENST00000520951.1:c.563A>G ENSP00000430074.1:p.Asp188Gly
ENST00000522510.5:c.404A>G ENSP00000430780.1:p.Asp135Gly
ENST00000523368.5:c.404A>G ENSP00000430041.1:p.Asp135Gly
NM_001142462.2:c.404A>G NP_001135934.1:p.Asp135Gly
NM_001286841.1:c.767A>G NP_001273770.1:p.Asp256Gly
NM_053001.3:c.404A>G NP_443727.2:p.Asp135Gly
XM_005250778.3:c.767A>G XP_005250835.1:p.Asp256Gly
XM_006716504.2:c.404A>G XP_006716567.1:p.Asp135Gly
XM_006716505.2:c.260A>G XP_006716568.1:p.Asp87Gly
XM_011516825.1:c.575A>G XP_011515127.1:p.Asp192Gly
XM_011516826.1:c.563A>G XP_011515128.1:p.Asp188Gly
XM_011516827.1:c.404A>G XP_011515129.1:p.Asp135Gly
XM_005250778.4:c.767A>G XP_005250835.1:p.Asp256Gly
XM_011516825.2:c.575A>G XP_011515127.1:p.Asp192Gly
XM_011516826.2:c.563A>G XP_011515128.1:p.Asp188Gly
XM_011516827.2:c.404A>G XP_011515129.1:p.Asp135Gly
XM_017013018.1:c.404A>G XP_016868507.1:p.Asp135Gly
NM_001142462.3:c.404A>G MANE Select NP_001135934.1:p.Asp135Gly
NM_001286841.2:c.767A>G NP_001273770.1:p.Asp256Gly
NM_053001.4:c.404A>G NP_443727.2:p.Asp135Gly
NM_001394683.1:c.260A>G NP_001381612.1:p.Asp87Gly