Canonical Allele Identifier: CA1871334977
Gene: ELP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108893945C= , CM000671.2:g.108893945C= GRCh38
NC_000009.11:g.111656225C= , CM000671.1:g.111656225C= GRCh37
NC_000009.10:g.110696046C= NCBI36
NG_008788.1:g.45384G= , LRG_251:g.45384G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374647.10:c.2858G= MANE Select ENSP00000363779.5:p.Cys953=
ENST00000495759.6:c.*1468G= ENSP00000433514.2:n.*1468G=
ENST00000674535.1:c.2858G= ENSP00000502142.1:p.Cys953=
ENST00000674704.1:n.5943G=
ENST00000674836.1:n.3471G=
ENST00000674890.1:c.*93G= ENSP00000501870.1:n.*93G=
ENST00000674938.1:c.2516G= ENSP00000502427.1:p.Cys839=
ENST00000674948.1:c.2516G= ENSP00000501602.1:p.Cys839=
ENST00000675052.1:c.2858G= ENSP00000502664.1:p.Cys953=
ENST00000675078.1:c.2858G= ENSP00000501549.1:p.Cys953=
ENST00000675215.1:c.*2082G= ENSP00000502558.1:n.*2082G=
ENST00000675233.1:n.4685G=
ENST00000675321.1:c.2858G= ENSP00000502751.1:p.Cys953=
ENST00000675325.1:n.4815G=
ENST00000675335.1:c.2889G= ENSP00000502182.1:n.2889G=
ENST00000675400.1:n.4593G=
ENST00000675406.1:c.2858G= ENSP00000501893.1:p.Cys953=
ENST00000675458.1:c.2951G= ENSP00000501754.1:n.2951G=
ENST00000675507.1:n.4654G=
ENST00000675535.1:c.*485G= ENSP00000501667.1:n.*485G=
ENST00000675566.1:n.4716G=
ENST00000675602.1:n.5906G=
ENST00000675647.1:n.3163G=
ENST00000675711.1:c.2858G= ENSP00000502485.1:p.Cys953=
ENST00000675727.1:c.2858G= ENSP00000501722.1:p.Cys953=
ENST00000675748.1:n.4492G=
ENST00000675765.1:c.*241G= ENSP00000502640.1:n.*241G=
ENST00000675825.1:c.2858G= ENSP00000502632.1:p.Cys953=
ENST00000675877.1:n.3163G=
ENST00000675893.1:c.*3927G= ENSP00000502001.1:n.*3927G=
ENST00000675943.1:n.6473G=
ENST00000675979.1:c.*2101G= ENSP00000502208.1:n.*2101G=
ENST00000676044.1:c.*518G= ENSP00000502378.1:n.*518G=
ENST00000676086.1:n.4643G=
ENST00000676121.1:n.4686G=
ENST00000676237.1:c.2759G= ENSP00000501828.1:p.Cys920=
ENST00000676416.1:c.2516G= ENSP00000501660.1:p.Cys839=
ENST00000676424.1:n.4654G=
ENST00000676429.1:n.7327G=
ENST00000374647.9:c.2858G= ENSP00000363779.5:p.Cys953=
ENST00000537196.1:c.1811G= ENSP00000439367.1:p.Cys604=
NM_003640.3:c.2858G= , LRG_251t1:c.2858G= NP_003631.2:p.Cys953=
XM_005252285.2:c.2516G= XP_005252342.1:p.Cys839=
XM_011519136.1:c.2858G= XP_011517438.1:p.Cys953=
XM_011519137.1:c.2516G= XP_011517439.1:p.Cys839=
XR_929859.1:n.3236G=
NM_001318360.1:c.2516G= NP_001305289.1:p.Cys839=
NM_001330749.1:c.1811G= NP_001317678.1:p.Cys604=
NM_003640.4:c.2858G= NP_003631.2:p.Cys953=
XM_011519136.2:c.2858G= XP_011517438.1:p.Cys953=
XR_929859.3:n.3247G=
NM_003640.5:c.2858G= MANE Select NP_003631.2:p.Cys953=
NM_001318360.2:c.2516G= NP_001305289.1:p.Cys839=
NM_001330749.2:c.1811G= NP_001317678.1:p.Cys604=