Canonical Allele Identifier: CA1871328638
Gene: ELP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108879554T= , CM000671.2:g.108879554T= GRCh38
NC_000009.11:g.111641834T= , CM000671.1:g.111641834T= GRCh37
NC_000009.10:g.110681655T= NCBI36
NG_008788.1:g.59775A= , LRG_251:g.59775A=

Transcript Alleles

HGVS Amino-acid change
ENST00000374647.10:c.3464A= MANE Select ENSP00000363779.5:p.Asp1155=
ENST00000495759.6:c.*2074A= ENSP00000433514.2:n.*2074A=
ENST00000674535.1:c.3464A= ENSP00000502142.1:p.Asp1155=
ENST00000674704.1:n.6549A=
ENST00000674740.1:n.347A=
ENST00000674836.1:n.4077A=
ENST00000674890.1:c.*699A= ENSP00000501870.1:n.*699A=
ENST00000674938.1:c.3122A= ENSP00000502427.1:p.Asp1041=
ENST00000674948.1:c.3122A= ENSP00000501602.1:p.Asp1041=
ENST00000675052.1:c.3464A= ENSP00000502664.1:p.Asp1155=
ENST00000675062.1:n.510A=
ENST00000675078.1:c.3464A= ENSP00000501549.1:p.Asp1155=
ENST00000675215.1:c.*2688A= ENSP00000502558.1:n.*2688A=
ENST00000675233.1:n.5291A=
ENST00000675321.1:c.3460+498A= ENSP00000502751.1:n.3460+498A=
ENST00000675325.1:n.5421A=
ENST00000675335.1:c.3495A= ENSP00000502182.1:n.3495A=
ENST00000675400.1:n.5316A=
ENST00000675406.1:c.3464A= ENSP00000501893.1:p.Asp1155=
ENST00000675458.1:c.3557A= ENSP00000501754.1:n.3557A=
ENST00000675507.1:n.5260A=
ENST00000675535.1:c.*1091A= ENSP00000501667.1:n.*1091A=
ENST00000675566.1:n.5322A=
ENST00000675580.1:n.617A=
ENST00000675602.1:n.6512A=
ENST00000675647.1:n.4628A=
ENST00000675711.1:c.3581A= ENSP00000502485.1:n.3581A=
ENST00000675727.1:c.3464A= ENSP00000501722.1:p.Asp1155=
ENST00000675748.1:n.5098A=
ENST00000675765.1:c.*847A= ENSP00000502640.1:n.*847A=
ENST00000675825.1:c.3506A= ENSP00000502632.1:p.Asp1169=
ENST00000675877.1:n.5308A=
ENST00000675893.1:c.*4533A= ENSP00000502001.1:n.*4533A=
ENST00000675943.1:n.7079A=
ENST00000675979.1:c.*2707A= ENSP00000502208.1:n.*2707A=
ENST00000676044.1:c.*1124A= ENSP00000502378.1:n.*1124A=
ENST00000676086.1:n.5249A=
ENST00000676121.1:n.5292A=
ENST00000676162.1:n.193A=
ENST00000676237.1:c.3407A= ENSP00000501828.1:p.Asp1136=
ENST00000676416.1:c.3164A= ENSP00000501660.1:p.Asp1055=
ENST00000676424.1:n.5302A=
ENST00000676429.1:n.7933A=
ENST00000374647.9:c.3464A= ENSP00000363779.5:p.Asp1155=
ENST00000467959.1:n.344A=
ENST00000495759.5:c.604A=
ENST00000537196.1:c.2417A= ENSP00000439367.1:p.Asp806=
NM_003640.3:c.3464A= , LRG_251t1:c.3464A= NP_003631.2:p.Asp1155=
XM_005252285.2:c.3122A= XP_005252342.1:p.Asp1041=
XM_011519136.1:c.3506A= XP_011517438.1:p.Asp1169=
XM_011519137.1:c.3164A= XP_011517439.1:p.Asp1055=
NM_001318360.1:c.3122A= NP_001305289.1:p.Asp1041=
NM_001330749.1:c.2417A= NP_001317678.1:p.Asp806=
NM_003640.4:c.3464A= NP_003631.2:p.Asp1155=
XM_011519136.2:c.3506A= XP_011517438.1:p.Asp1169=
XR_929859.3:n.3853A=
NM_003640.5:c.3464A= MANE Select NP_003631.2:p.Asp1155=
NM_001318360.2:c.3122A= NP_001305289.1:p.Asp1041=
NM_001330749.2:c.2417A= NP_001317678.1:p.Asp806=