Canonical Allele Identifier: CA1871328593
Gene: ELP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108879467T= , CM000671.2:g.108879467T= GRCh38
NC_000009.11:g.111641747T= , CM000671.1:g.111641747T= GRCh37
NC_000009.10:g.110681568T= NCBI36
NG_008788.1:g.59862A= , LRG_251:g.59862A=

Transcript Alleles

HGVS Amino-acid change
ENST00000374647.10:c.3551A= MANE Select ENSP00000363779.5:p.His1184=
ENST00000495759.6:c.*2161A= ENSP00000433514.2:n.*2161A=
ENST00000674535.1:c.3551A= ENSP00000502142.1:p.His1184=
ENST00000674704.1:n.6636A=
ENST00000674740.1:n.434A=
ENST00000674836.1:n.4164A=
ENST00000674890.1:c.*786A= ENSP00000501870.1:n.*786A=
ENST00000674938.1:c.3209A= ENSP00000502427.1:p.His1070=
ENST00000674948.1:c.3209A= ENSP00000501602.1:p.His1070=
ENST00000675052.1:c.3551A= ENSP00000502664.1:p.His1184=
ENST00000675062.1:n.597A=
ENST00000675078.1:c.3551A= ENSP00000501549.1:p.His1184=
ENST00000675215.1:c.*2775A= ENSP00000502558.1:n.*2775A=
ENST00000675233.1:n.5378A=
ENST00000675321.1:c.3460+585A= ENSP00000502751.1:n.3460+585A=
ENST00000675325.1:n.5508A=
ENST00000675335.1:c.3582A= ENSP00000502182.1:n.3582A=
ENST00000675400.1:n.5403A=
ENST00000675406.1:c.3551A= ENSP00000501893.1:p.His1184=
ENST00000675458.1:c.3644A= ENSP00000501754.1:n.3644A=
ENST00000675507.1:n.5347A=
ENST00000675535.1:c.*1178A= ENSP00000501667.1:n.*1178A=
ENST00000675566.1:n.5409A=
ENST00000675580.1:n.704A=
ENST00000675602.1:n.6599A=
ENST00000675647.1:n.4715A=
ENST00000675711.1:c.3668A= ENSP00000502485.1:n.3668A=
ENST00000675727.1:c.3551A= ENSP00000501722.1:p.His1184=
ENST00000675748.1:n.5185A=
ENST00000675765.1:c.*934A= ENSP00000502640.1:n.*934A=
ENST00000675825.1:c.3593A= ENSP00000502632.1:p.His1198=
ENST00000675877.1:n.5395A=
ENST00000675893.1:c.*4620A= ENSP00000502001.1:n.*4620A=
ENST00000675943.1:n.7166A=
ENST00000675979.1:c.*2794A= ENSP00000502208.1:n.*2794A=
ENST00000676044.1:c.*1211A= ENSP00000502378.1:n.*1211A=
ENST00000676086.1:n.5336A=
ENST00000676121.1:n.5379A=
ENST00000676162.1:n.280A=
ENST00000676237.1:c.3494A= ENSP00000501828.1:p.His1165=
ENST00000676416.1:c.3251A= ENSP00000501660.1:p.His1084=
ENST00000676424.1:n.5389A=
ENST00000676429.1:n.8020A=
ENST00000374647.9:c.3551A= ENSP00000363779.5:p.His1184=
ENST00000467959.1:n.431A=
ENST00000495759.5:c.691A=
ENST00000537196.1:c.2504A= ENSP00000439367.1:p.His835=
NM_003640.3:c.3551A= , LRG_251t1:c.3551A= NP_003631.2:p.His1184=
XM_005252285.2:c.3209A= XP_005252342.1:p.His1070=
XM_011519136.1:c.3593A= XP_011517438.1:p.His1198=
XM_011519137.1:c.3251A= XP_011517439.1:p.His1084=
NM_001318360.1:c.3209A= NP_001305289.1:p.His1070=
NM_001330749.1:c.2504A= NP_001317678.1:p.His835=
NM_003640.4:c.3551A= NP_003631.2:p.His1184=
XM_011519136.2:c.3593A= XP_011517438.1:p.His1198=
XR_929859.3:n.3940A=
NM_003640.5:c.3551A= MANE Select NP_003631.2:p.His1184=
NM_001318360.2:c.3209A= NP_001305289.1:p.His1070=
NM_001330749.2:c.2504A= NP_001317678.1:p.His835=