Canonical Allele Identifier: CA2130972
Community Standard Title: NM_015311.3(OBSL1):c.3078G>C (p.Gly1026=)
Gene: OBSL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219559373C>G , CM000664.2:g.219559373C>G GRCh38
NC_000002.11:g.220424095C>G , CM000664.1:g.220424095C>G GRCh37
NC_000002.10:g.220132339C>G NCBI36
NG_016977.1:g.17174G>C

Transcript Alleles

HGVS Amino-acid Change
NM_015311.3:c.3078G>C MANE Select NP_056126.1:p.Gly1026=
ENST00000404537.6:c.3078G>C MANE Select ENSP00000385636.1:p.Gly1026=
NM_001173431.1:c.3078G>C NP_001166902.1:p.Gly1026=
NM_001173431.2:c.3078G>C NP_001166902.1:p.Gly1026=
NM_015311.2:c.3078G>C NP_056126.1:p.Gly1026=
ENST00000373876.5:c.3078G>C ENSP00000362983.1:p.Gly1026=
ENST00000404537.5:c.3078G>C ENSP00000385636.1:p.Gly1026=
ENST00000456147.1:c.59G>C
ENST00000465149.1:n.2585G>C
ENST00000603926.5:c.3078G>C ENSP00000474519.1:p.Gly1026=
ENST00000604031.5:c.236G>C
XM_005246424.3:c.3078G>C XP_005246481.1:p.Gly1026=
XM_005246427.3:c.3078G>C XP_005246484.1:p.Gly1026=
XM_011510854.1:c.3078G>C XP_011509156.1:p.Gly1026=
XM_011510855.1:c.3078G>C XP_011509157.1:p.Gly1026=
XM_011510856.1:c.3078G>C XP_011509158.1:p.Gly1026=
XM_011510857.1:c.3078G>C XP_011509159.1:p.Gly1026=
XM_011510857.2:c.3078G>C XP_011509159.1:p.Gly1026=
XM_011510858.1:c.3078G>C XP_011509160.1:p.Gly1026=
XM_011510859.1:c.3078G>C XP_011509161.1:p.Gly1026=
XM_011510860.1:c.3078G>C XP_011509162.1:p.Gly1026=
XM_011510861.1:c.3078G>C XP_011509163.1:p.Gly1026=
XM_011510862.1:c.3078G>C XP_011509164.1:p.Gly1026=
XM_011510863.1:c.3078G>C XP_011509165.1:p.Gly1026=
XM_011510863.3:c.3078G>C XP_011509165.1:p.Gly1026=
XM_011510864.1:c.3078G>C XP_011509166.1:p.Gly1026=
XM_011510864.2:c.3078G>C XP_011509166.1:p.Gly1026=
XM_011510865.1:c.3078G>C XP_011509167.1:p.Gly1026=
XM_011510865.2:c.3078G>C XP_011509167.1:p.Gly1026=
XM_011510866.1:c.3078G>C XP_011509168.1:p.Gly1026=
XM_011510866.2:c.3078G>C XP_011509168.1:p.Gly1026=
XM_017003696.2:c.3078G>C XP_016859185.1:p.Gly1026=
XM_017003697.2:c.3078G>C XP_016859186.1:p.Gly1026=
XM_017003698.1:c.3078G>C XP_016859187.1:p.Gly1026=
XM_017003699.1:c.3078G>C XP_016859188.1:p.Gly1026=
XM_017003700.1:c.3078G>C XP_016859189.1:p.Gly1026=