Canonical Allele Identifier: CA1871337579
Gene: ELP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108899837C= , CM000671.2:g.108899837C= GRCh38
NC_000009.11:g.111662117C= , CM000671.1:g.111662117C= GRCh37
NC_000009.10:g.110701938C= NCBI36
NG_008788.1:g.39492G= , LRG_251:g.39492G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374647.10:c.2189G= MANE Select ENSP00000363779.5:p.Arg730=
ENST00000495759.6:c.*799G= ENSP00000433514.2:n.*799G=
ENST00000674535.1:c.2189G= ENSP00000502142.1:p.Arg730=
ENST00000674704.1:n.3996G=
ENST00000674836.1:n.2494G=
ENST00000674890.1:c.2189G= ENSP00000501870.1:p.Arg730=
ENST00000674938.1:c.1847G= ENSP00000502427.1:p.Arg616=
ENST00000674948.1:c.1847G= ENSP00000501602.1:p.Arg616=
ENST00000675052.1:c.2189G= ENSP00000502664.1:p.Arg730=
ENST00000675078.1:c.2189G= ENSP00000501549.1:p.Arg730=
ENST00000675215.1:c.*1413G= ENSP00000502558.1:n.*1413G=
ENST00000675233.1:n.4016G=
ENST00000675321.1:c.2189G= ENSP00000502751.1:p.Arg730=
ENST00000675325.1:n.3985G=
ENST00000675335.1:c.2220G= ENSP00000502182.1:n.2220G=
ENST00000675400.1:n.3862G=
ENST00000675406.1:c.2189G= ENSP00000501893.1:p.Arg730=
ENST00000675458.1:c.2282G= ENSP00000501754.1:n.2282G=
ENST00000675507.1:n.3985G=
ENST00000675535.1:c.2189G= ENSP00000501667.1:p.Arg730=
ENST00000675566.1:n.3985G=
ENST00000675602.1:n.5237G=
ENST00000675647.1:n.2494G=
ENST00000675711.1:c.2189G= ENSP00000502485.1:p.Arg730=
ENST00000675727.1:c.2189G= ENSP00000501722.1:p.Arg730=
ENST00000675748.1:n.3823G=
ENST00000675765.1:c.2189G= ENSP00000502640.1:p.Arg730=
ENST00000675825.1:c.2189G= ENSP00000502632.1:p.Arg730=
ENST00000675877.1:n.2494G=
ENST00000675893.1:c.*3258G= ENSP00000502001.1:n.*3258G=
ENST00000675943.1:n.5804G=
ENST00000675979.1:c.*1432G= ENSP00000502208.1:n.*1432G=
ENST00000676044.1:c.2189G= ENSP00000502378.1:p.Arg730=
ENST00000676086.1:n.3974G=
ENST00000676121.1:n.4017G=
ENST00000676237.1:c.2090G= ENSP00000501828.1:p.Arg697=
ENST00000676416.1:c.1847G= ENSP00000501660.1:p.Arg616=
ENST00000676424.1:n.3985G=
ENST00000676429.1:n.6658G=
ENST00000374647.9:c.2189G= ENSP00000363779.5:p.Arg730=
ENST00000537196.1:c.1142G= ENSP00000439367.1:p.Arg381=
NM_003640.3:c.2189G= , LRG_251t1:c.2189G= NP_003631.2:p.Arg730=
XM_005252285.2:c.1847G= XP_005252342.1:p.Arg616=
XM_011519136.1:c.2189G= XP_011517438.1:p.Arg730=
XM_011519137.1:c.1847G= XP_011517439.1:p.Arg616=
XR_929859.1:n.2505G=
NM_001318360.1:c.1847G= NP_001305289.1:p.Arg616=
NM_001330749.1:c.1142G= NP_001317678.1:p.Arg381=
NM_003640.4:c.2189G= NP_003631.2:p.Arg730=
XM_011519136.2:c.2189G= XP_011517438.1:p.Arg730=
XR_929859.3:n.2516G=
NM_003640.5:c.2189G= MANE Select NP_003631.2:p.Arg730=
NM_001318360.2:c.1847G= NP_001305289.1:p.Arg616=
NM_001330749.2:c.1142G= NP_001317678.1:p.Arg381=