Canonical Allele Identifier: CA1871335001
Gene: ELP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108894002A= , CM000671.2:g.108894002A= GRCh38
NC_000009.11:g.111656282A= , CM000671.1:g.111656282A= GRCh37
NC_000009.10:g.110696103A= NCBI36
NG_008788.1:g.45327T= , LRG_251:g.45327T=

Transcript Alleles

HGVS Amino-acid change
ENST00000374647.10:c.2801T= MANE Select ENSP00000363779.5:p.Phe934=
ENST00000495759.6:c.*1411T= ENSP00000433514.2:n.*1411T=
ENST00000674535.1:c.2801T= ENSP00000502142.1:p.Phe934=
ENST00000674704.1:n.5886T=
ENST00000674836.1:n.3414T=
ENST00000674890.1:c.*36T= ENSP00000501870.1:n.*36T=
ENST00000674938.1:c.2459T= ENSP00000502427.1:p.Phe820=
ENST00000674948.1:c.2459T= ENSP00000501602.1:p.Phe820=
ENST00000675052.1:c.2801T= ENSP00000502664.1:p.Phe934=
ENST00000675078.1:c.2801T= ENSP00000501549.1:p.Phe934=
ENST00000675215.1:c.*2025T= ENSP00000502558.1:n.*2025T=
ENST00000675233.1:n.4628T=
ENST00000675321.1:c.2801T= ENSP00000502751.1:p.Phe934=
ENST00000675325.1:n.4758T=
ENST00000675335.1:c.2832T= ENSP00000502182.1:n.2832T=
ENST00000675400.1:n.4536T=
ENST00000675406.1:c.2801T= ENSP00000501893.1:p.Phe934=
ENST00000675458.1:c.2894T= ENSP00000501754.1:n.2894T=
ENST00000675507.1:n.4597T=
ENST00000675535.1:c.*428T= ENSP00000501667.1:n.*428T=
ENST00000675566.1:n.4659T=
ENST00000675602.1:n.5849T=
ENST00000675647.1:n.3106T=
ENST00000675711.1:c.2801T= ENSP00000502485.1:p.Phe934=
ENST00000675727.1:c.2801T= ENSP00000501722.1:p.Phe934=
ENST00000675748.1:n.4435T=
ENST00000675765.1:c.*184T= ENSP00000502640.1:n.*184T=
ENST00000675825.1:c.2801T= ENSP00000502632.1:p.Phe934=
ENST00000675877.1:n.3106T=
ENST00000675893.1:c.*3870T= ENSP00000502001.1:n.*3870T=
ENST00000675943.1:n.6416T=
ENST00000675979.1:c.*2044T= ENSP00000502208.1:n.*2044T=
ENST00000676044.1:c.*461T= ENSP00000502378.1:n.*461T=
ENST00000676086.1:n.4586T=
ENST00000676121.1:n.4629T=
ENST00000676237.1:c.2702T= ENSP00000501828.1:p.Phe901=
ENST00000676416.1:c.2459T= ENSP00000501660.1:p.Phe820=
ENST00000676424.1:n.4597T=
ENST00000676429.1:n.7270T=
ENST00000374647.9:c.2801T= ENSP00000363779.5:p.Phe934=
ENST00000537196.1:c.1754T= ENSP00000439367.1:p.Phe585=
NM_003640.3:c.2801T= , LRG_251t1:c.2801T= NP_003631.2:p.Phe934=
XM_005252285.2:c.2459T= XP_005252342.1:p.Phe820=
XM_011519136.1:c.2801T= XP_011517438.1:p.Phe934=
XM_011519137.1:c.2459T= XP_011517439.1:p.Phe820=
XR_929859.1:n.3179T=
NM_001318360.1:c.2459T= NP_001305289.1:p.Phe820=
NM_001330749.1:c.1754T= NP_001317678.1:p.Phe585=
NM_003640.4:c.2801T= NP_003631.2:p.Phe934=
XM_011519136.2:c.2801T= XP_011517438.1:p.Phe934=
XR_929859.3:n.3190T=
NM_003640.5:c.2801T= MANE Select NP_003631.2:p.Phe934=
NM_001318360.2:c.2459T= NP_001305289.1:p.Phe820=
NM_001330749.2:c.1754T= NP_001317678.1:p.Phe585=