Canonical Allele Identifier: CA1871328592
Gene: ELP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108879465T= , CM000671.2:g.108879465T= GRCh38
NC_000009.11:g.111641745T= , CM000671.1:g.111641745T= GRCh37
NC_000009.10:g.110681566T= NCBI36
NG_008788.1:g.59864A= , LRG_251:g.59864A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374647.10:c.3553A= MANE Select ENSP00000363779.5:p.Ser1185=
ENST00000495759.6:c.*2163A= ENSP00000433514.2:n.*2163A=
ENST00000674535.1:c.3553A= ENSP00000502142.1:p.Ser1185=
ENST00000674704.1:n.6638A=
ENST00000674740.1:n.436A=
ENST00000674836.1:n.4166A=
ENST00000674890.1:c.*788A= ENSP00000501870.1:n.*788A=
ENST00000674938.1:c.3211A= ENSP00000502427.1:p.Ser1071=
ENST00000674948.1:c.3211A= ENSP00000501602.1:p.Ser1071=
ENST00000675052.1:c.3553A= ENSP00000502664.1:p.Ser1185=
ENST00000675062.1:n.599A=
ENST00000675078.1:c.3553A= ENSP00000501549.1:p.Ser1185=
ENST00000675215.1:c.*2777A= ENSP00000502558.1:n.*2777A=
ENST00000675233.1:n.5380A=
ENST00000675321.1:c.3460+587A= ENSP00000502751.1:n.3460+587A=
ENST00000675325.1:n.5510A=
ENST00000675335.1:c.3584A= ENSP00000502182.1:n.3584A=
ENST00000675400.1:n.5405A=
ENST00000675406.1:c.3553A= ENSP00000501893.1:p.Ser1185=
ENST00000675458.1:c.3646A= ENSP00000501754.1:n.3646A=
ENST00000675507.1:n.5349A=
ENST00000675535.1:c.*1180A= ENSP00000501667.1:n.*1180A=
ENST00000675566.1:n.5411A=
ENST00000675580.1:n.706A=
ENST00000675602.1:n.6601A=
ENST00000675647.1:n.4717A=
ENST00000675711.1:c.3670A= ENSP00000502485.1:n.3670A=
ENST00000675727.1:c.3553A= ENSP00000501722.1:p.Ser1185=
ENST00000675748.1:n.5187A=
ENST00000675765.1:c.*936A= ENSP00000502640.1:n.*936A=
ENST00000675825.1:c.3595A= ENSP00000502632.1:p.Ser1199=
ENST00000675877.1:n.5397A=
ENST00000675893.1:c.*4622A= ENSP00000502001.1:n.*4622A=
ENST00000675943.1:n.7168A=
ENST00000675979.1:c.*2796A= ENSP00000502208.1:n.*2796A=
ENST00000676044.1:c.*1213A= ENSP00000502378.1:n.*1213A=
ENST00000676086.1:n.5338A=
ENST00000676121.1:n.5381A=
ENST00000676162.1:n.282A=
ENST00000676237.1:c.3496A= ENSP00000501828.1:p.Ser1166=
ENST00000676416.1:c.3253A= ENSP00000501660.1:p.Ser1085=
ENST00000676424.1:n.5391A=
ENST00000676429.1:n.8022A=
ENST00000374647.9:c.3553A= ENSP00000363779.5:p.Ser1185=
ENST00000467959.1:n.433A=
ENST00000495759.5:c.693A=
ENST00000537196.1:c.2506A= ENSP00000439367.1:p.Ser836=
NM_003640.3:c.3553A= , LRG_251t1:c.3553A= NP_003631.2:p.Ser1185=
XM_005252285.2:c.3211A= XP_005252342.1:p.Ser1071=
XM_011519136.1:c.3595A= XP_011517438.1:p.Ser1199=
XM_011519137.1:c.3253A= XP_011517439.1:p.Ser1085=
NM_001318360.1:c.3211A= NP_001305289.1:p.Ser1071=
NM_001330749.1:c.2506A= NP_001317678.1:p.Ser836=
NM_003640.4:c.3553A= NP_003631.2:p.Ser1185=
XM_011519136.2:c.3595A= XP_011517438.1:p.Ser1199=
XR_929859.3:n.3942A=
NM_003640.5:c.3553A= MANE Select NP_003631.2:p.Ser1185=
NM_001318360.2:c.3211A= NP_001305289.1:p.Ser1071=
NM_001330749.2:c.2506A= NP_001317678.1:p.Ser836=