Canonical Allele Identifier: CA1871335004
Gene: ELP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108894006G= , CM000671.2:g.108894006G= GRCh38
NC_000009.11:g.111656286G= , CM000671.1:g.111656286G= GRCh37
NC_000009.10:g.110696107G= NCBI36
NG_008788.1:g.45323C= , LRG_251:g.45323C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374647.10:c.2797C= MANE Select ENSP00000363779.5:p.Arg933=
ENST00000495759.6:c.*1407C= ENSP00000433514.2:n.*1407C=
ENST00000674535.1:c.2797C= ENSP00000502142.1:p.Arg933=
ENST00000674704.1:n.5882C=
ENST00000674836.1:n.3410C=
ENST00000674890.1:c.*32C= ENSP00000501870.1:n.*32C=
ENST00000674938.1:c.2455C= ENSP00000502427.1:p.Arg819=
ENST00000674948.1:c.2455C= ENSP00000501602.1:p.Arg819=
ENST00000675052.1:c.2797C= ENSP00000502664.1:p.Arg933=
ENST00000675078.1:c.2797C= ENSP00000501549.1:p.Arg933=
ENST00000675215.1:c.*2021C= ENSP00000502558.1:n.*2021C=
ENST00000675233.1:n.4624C=
ENST00000675321.1:c.2797C= ENSP00000502751.1:p.Arg933=
ENST00000675325.1:n.4754C=
ENST00000675335.1:c.2828C= ENSP00000502182.1:n.2828C=
ENST00000675400.1:n.4532C=
ENST00000675406.1:c.2797C= ENSP00000501893.1:p.Arg933=
ENST00000675458.1:c.2890C= ENSP00000501754.1:n.2890C=
ENST00000675507.1:n.4593C=
ENST00000675535.1:c.*424C= ENSP00000501667.1:n.*424C=
ENST00000675566.1:n.4655C=
ENST00000675602.1:n.5845C=
ENST00000675647.1:n.3102C=
ENST00000675711.1:c.2797C= ENSP00000502485.1:p.Arg933=
ENST00000675727.1:c.2797C= ENSP00000501722.1:p.Arg933=
ENST00000675748.1:n.4431C=
ENST00000675765.1:c.*180C= ENSP00000502640.1:n.*180C=
ENST00000675825.1:c.2797C= ENSP00000502632.1:p.Arg933=
ENST00000675877.1:n.3102C=
ENST00000675893.1:c.*3866C= ENSP00000502001.1:n.*3866C=
ENST00000675943.1:n.6412C=
ENST00000675979.1:c.*2040C= ENSP00000502208.1:n.*2040C=
ENST00000676044.1:c.*457C= ENSP00000502378.1:n.*457C=
ENST00000676086.1:n.4582C=
ENST00000676121.1:n.4625C=
ENST00000676237.1:c.2698C= ENSP00000501828.1:p.Arg900=
ENST00000676416.1:c.2455C= ENSP00000501660.1:p.Arg819=
ENST00000676424.1:n.4593C=
ENST00000676429.1:n.7266C=
ENST00000374647.9:c.2797C= ENSP00000363779.5:p.Arg933=
ENST00000537196.1:c.1750C= ENSP00000439367.1:p.Arg584=
NM_003640.3:c.2797C= , LRG_251t1:c.2797C= NP_003631.2:p.Arg933=
XM_005252285.2:c.2455C= XP_005252342.1:p.Arg819=
XM_011519136.1:c.2797C= XP_011517438.1:p.Arg933=
XM_011519137.1:c.2455C= XP_011517439.1:p.Arg819=
XR_929859.1:n.3175C=
NM_001318360.1:c.2455C= NP_001305289.1:p.Arg819=
NM_001330749.1:c.1750C= NP_001317678.1:p.Arg584=
NM_003640.4:c.2797C= NP_003631.2:p.Arg933=
XM_011519136.2:c.2797C= XP_011517438.1:p.Arg933=
XR_929859.3:n.3186C=
NM_003640.5:c.2797C= MANE Select NP_003631.2:p.Arg933=
NM_001318360.2:c.2455C= NP_001305289.1:p.Arg819=
NM_001330749.2:c.1750C= NP_001317678.1:p.Arg584=