Canonical Allele Identifier: CA10171733
Community Standard Title: NM_005243.4(EWSR1):c.1393G>A (p.Gly465Ser)
Gene: EWSR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29297925G>A , CM000684.2:g.29297925G>A GRCh38
NC_000022.10:g.29693915G>A , CM000684.1:g.29693915G>A GRCh37
NC_000022.9:g.28023915G>A NCBI36
NG_023240.1:g.34918G>A

Transcript Alleles

HGVS Amino-acid Change
NM_005243.4:c.1393G>A MANE Select NP_005234.1:p.Gly465Ser
ENST00000397938.7:c.1393G>A MANE Select ENSP00000381031.2:p.Gly465Ser
NM_001163285.1:c.1390G>A NP_001156757.1:p.Gly464Ser
NM_001163285.2:c.1390G>A NP_001156757.1:p.Gly464Ser
NM_001163286.1:c.1225G>A NP_001156758.1:p.Gly409Ser
NM_001163286.2:c.1225G>A NP_001156758.1:p.Gly409Ser
NM_005243.3:c.1393G>A NP_005234.1:p.Gly465Ser
NM_013986.3:c.1408G>A NP_053733.2:p.Gly470Ser
NM_013986.4:c.1408G>A NP_053733.2:p.Gly470Ser
ENST00000331029.11:c.1279G>A ENSP00000330516.7:p.Gly427Ser
ENST00000332035.10:c.1225G>A ENSP00000331699.6:p.Gly409Ser
ENST00000332050.10:c.1285G>A ENSP00000330896.7:p.Gly429Ser
ENST00000360091.3:c.359G>A
ENST00000397938.6:c.1393G>A ENSP00000381031.2:p.Gly465Ser
ENST00000406548.5:c.1390G>A ENSP00000385726.1:p.Gly464Ser
ENST00000414183.6:c.1408G>A ENSP00000400142.2:p.Gly470Ser
ENST00000469669.5:n.1688G>A
ENST00000479135.5:n.6343G>A
ENST00000483629.5:n.589G>A
ENST00000610553.1:n.942G>A
ENST00000629659.2:c.1177G>A ENSP00000486709.1:p.Gly393Ser
XM_005261389.2:c.1393G>A XP_005261446.1:p.Gly465Ser
XM_005261389.4:c.1393G>A XP_005261446.1:p.Gly465Ser
XM_005261390.3:c.1225G>A XP_005261447.1:p.Gly409Ser
XM_005261390.4:c.1225G>A XP_005261447.1:p.Gly409Ser
XM_011529995.1:c.1396G>A XP_011528297.1:p.Gly466Ser
XM_011529995.3:c.1396G>A XP_011528297.1:p.Gly466Ser
XM_011529996.1:c.1393G>A XP_011528298.1:p.Gly465Ser
XM_011529996.3:c.1393G>A XP_011528298.1:p.Gly465Ser
XM_011529997.1:c.1396G>A XP_011528299.1:p.Gly466Ser
XM_011529997.2:c.1396G>A XP_011528299.1:p.Gly466Ser
XM_011529998.1:c.1393G>A XP_011528300.1:p.Gly465Ser
XM_011529998.2:c.1393G>A XP_011528300.1:p.Gly465Ser
XM_011529999.1:c.1396G>A XP_011528301.1:p.Gly466Ser
XM_011529999.3:c.1396G>A XP_011528301.1:p.Gly466Ser
XM_011530000.1:c.1396G>A XP_011528302.1:p.Gly466Ser
XM_011530000.2:c.1396G>A XP_011528302.1:p.Gly466Ser
XM_011530001.1:c.1228G>A XP_011528303.1:p.Gly410Ser
XM_011530001.2:c.1228G>A XP_011528303.1:p.Gly410Ser
XM_011530002.1:c.1177G>A XP_011528304.1:p.Gly393Ser
XM_011530002.3:c.1177G>A XP_011528304.1:p.Gly393Ser
XM_017028644.2:c.1390G>A XP_016884133.1:p.Gly464Ser
XM_017028645.2:c.1393G>A XP_016884134.1:p.Gly465Ser
XM_017028646.2:c.1393G>A XP_016884135.1:p.Gly465Ser
XM_017028647.2:c.1390G>A XP_016884136.1:p.Gly464Ser
XM_017028648.2:c.1390G>A XP_016884137.1:p.Gly464Ser
XM_017028649.2:c.1298-808G>A XP_016884138.1:n.1298-808G>A
XM_017028650.2:c.1298-808G>A XP_016884139.1:n.1298-808G>A
XM_017028651.2:c.1295-808G>A XP_016884140.1:n.1295-808G>A
XM_017028652.2:c.1295-808G>A XP_016884141.1:n.1295-808G>A
XM_017028653.2:c.1292-808G>A XP_016884142.1:n.1292-808G>A
XM_017028654.1:c.1225G>A XP_016884143.1:p.Gly409Ser
XM_017028655.1:c.1222G>A XP_016884144.1:p.Gly408Ser
XM_017028656.2:c.1295-808G>A XP_016884145.1:n.1295-808G>A
XM_017028657.2:c.1189G>A XP_016884146.1:p.Gly397Ser
XM_017028658.1:c.1225G>A XP_016884147.1:p.Gly409Ser
XM_017028659.1:c.1222G>A XP_016884148.1:p.Gly408Ser
XM_017028660.2:c.1292-808G>A XP_016884149.1:n.1292-808G>A
XM_017028661.2:c.1186G>A XP_016884150.1:p.Gly396Ser
XM_017028662.2:c.1222G>A XP_016884151.1:p.Gly408Ser
XM_017028663.1:c.1124-808G>A XP_016884152.1:n.1124-808G>A
XM_017028664.2:c.376G>A XP_016884153.1:p.Gly126Ser
XM_017028665.2:c.376G>A XP_016884154.1:p.Gly126Ser
XM_017028666.2:c.376G>A XP_016884155.1:p.Gly126Ser
XM_024452180.1:c.1177G>A XP_024307948.1:p.Gly393Ser
XM_024452181.1:c.1174G>A XP_024307949.1:p.Gly392Ser
XR_002958676.1:n.2880G>A