Canonical Allele Identifier: CA1871335006
Gene: ELP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108894010A= , CM000671.2:g.108894010A= GRCh38
NC_000009.11:g.111656290A= , CM000671.1:g.111656290A= GRCh37
NC_000009.10:g.110696111A= NCBI36
NG_008788.1:g.45319T= , LRG_251:g.45319T=

Transcript Alleles

HGVS Amino-acid change
ENST00000374647.10:c.2793T= MANE Select ENSP00000363779.5:p.Tyr931=
ENST00000495759.6:c.*1403T= ENSP00000433514.2:n.*1403T=
ENST00000674535.1:c.2793T= ENSP00000502142.1:p.Tyr931=
ENST00000674704.1:n.5878T=
ENST00000674836.1:n.3406T=
ENST00000674890.1:c.*28T= ENSP00000501870.1:n.*28T=
ENST00000674938.1:c.2451T= ENSP00000502427.1:p.Tyr817=
ENST00000674948.1:c.2451T= ENSP00000501602.1:p.Tyr817=
ENST00000675052.1:c.2793T= ENSP00000502664.1:p.Tyr931=
ENST00000675078.1:c.2793T= ENSP00000501549.1:p.Tyr931=
ENST00000675215.1:c.*2017T= ENSP00000502558.1:n.*2017T=
ENST00000675233.1:n.4620T=
ENST00000675321.1:c.2793T= ENSP00000502751.1:p.Tyr931=
ENST00000675325.1:n.4750T=
ENST00000675335.1:c.2824T= ENSP00000502182.1:n.2824T=
ENST00000675400.1:n.4528T=
ENST00000675406.1:c.2793T= ENSP00000501893.1:p.Tyr931=
ENST00000675458.1:c.2886T= ENSP00000501754.1:n.2886T=
ENST00000675507.1:n.4589T=
ENST00000675535.1:c.*420T= ENSP00000501667.1:n.*420T=
ENST00000675566.1:n.4651T=
ENST00000675602.1:n.5841T=
ENST00000675647.1:n.3098T=
ENST00000675711.1:c.2793T= ENSP00000502485.1:p.Tyr931=
ENST00000675727.1:c.2793T= ENSP00000501722.1:p.Tyr931=
ENST00000675748.1:n.4427T=
ENST00000675765.1:c.*176T= ENSP00000502640.1:n.*176T=
ENST00000675825.1:c.2793T= ENSP00000502632.1:p.Tyr931=
ENST00000675877.1:n.3098T=
ENST00000675893.1:c.*3862T= ENSP00000502001.1:n.*3862T=
ENST00000675943.1:n.6408T=
ENST00000675979.1:c.*2036T= ENSP00000502208.1:n.*2036T=
ENST00000676044.1:c.*453T= ENSP00000502378.1:n.*453T=
ENST00000676086.1:n.4578T=
ENST00000676121.1:n.4621T=
ENST00000676237.1:c.2694T= ENSP00000501828.1:p.Tyr898=
ENST00000676416.1:c.2451T= ENSP00000501660.1:p.Tyr817=
ENST00000676424.1:n.4589T=
ENST00000676429.1:n.7262T=
ENST00000374647.9:c.2793T= ENSP00000363779.5:p.Tyr931=
ENST00000537196.1:c.1746T= ENSP00000439367.1:p.Tyr582=
NM_003640.3:c.2793T= , LRG_251t1:c.2793T= NP_003631.2:p.Tyr931=
XM_005252285.2:c.2451T= XP_005252342.1:p.Tyr817=
XM_011519136.1:c.2793T= XP_011517438.1:p.Tyr931=
XM_011519137.1:c.2451T= XP_011517439.1:p.Tyr817=
XR_929859.1:n.3171T=
NM_001318360.1:c.2451T= NP_001305289.1:p.Tyr817=
NM_001330749.1:c.1746T= NP_001317678.1:p.Tyr582=
NM_003640.4:c.2793T= NP_003631.2:p.Tyr931=
XM_011519136.2:c.2793T= XP_011517438.1:p.Tyr931=
XR_929859.3:n.3182T=
NM_003640.5:c.2793T= MANE Select NP_003631.2:p.Tyr931=
NM_001318360.2:c.2451T= NP_001305289.1:p.Tyr817=
NM_001330749.2:c.1746T= NP_001317678.1:p.Tyr582=