Canonical Allele Identifier: CA1871332963
Gene: ELP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108889345T= , CM000671.2:g.108889345T= GRCh38
NC_000009.11:g.111651625T= , CM000671.1:g.111651625T= GRCh37
NC_000009.10:g.110691446T= NCBI36
NG_008788.1:g.49984A= , LRG_251:g.49984A=

Transcript Alleles

HGVS Amino-acid change
ENST00000374647.10:c.3209A= MANE Select ENSP00000363779.5:p.Glu1070=
ENST00000495759.6:c.*1819A= ENSP00000433514.2:n.*1819A=
ENST00000674535.1:c.3209A= ENSP00000502142.1:p.Glu1070=
ENST00000674704.1:n.6294A=
ENST00000674836.1:n.3822A=
ENST00000674890.1:c.*444A= ENSP00000501870.1:n.*444A=
ENST00000674938.1:c.2867A= ENSP00000502427.1:p.Glu956=
ENST00000674948.1:c.2867A= ENSP00000501602.1:p.Glu956=
ENST00000675052.1:c.3209A= ENSP00000502664.1:p.Glu1070=
ENST00000675078.1:c.3209A= ENSP00000501549.1:p.Glu1070=
ENST00000675215.1:c.*2433A= ENSP00000502558.1:n.*2433A=
ENST00000675233.1:n.5036A=
ENST00000675321.1:c.3209A= ENSP00000502751.1:p.Glu1070=
ENST00000675325.1:n.5166A=
ENST00000675335.1:c.3240A= ENSP00000502182.1:n.3240A=
ENST00000675400.1:n.4944A=
ENST00000675406.1:c.3209A= ENSP00000501893.1:p.Glu1070=
ENST00000675458.1:c.3302A= ENSP00000501754.1:n.3302A=
ENST00000675507.1:n.5005A=
ENST00000675535.1:c.*836A= ENSP00000501667.1:n.*836A=
ENST00000675566.1:n.5067A=
ENST00000675602.1:n.6257A=
ENST00000675647.1:n.4373A=
ENST00000675711.1:c.3209A= ENSP00000502485.1:p.Glu1070=
ENST00000675727.1:c.3209A= ENSP00000501722.1:p.Glu1070=
ENST00000675748.1:n.4843A=
ENST00000675765.1:c.*592A= ENSP00000502640.1:n.*592A=
ENST00000675825.1:c.3209A= ENSP00000502632.1:p.Glu1070=
ENST00000675877.1:n.3514A=
ENST00000675893.1:c.*4278A= ENSP00000502001.1:n.*4278A=
ENST00000675943.1:n.6824A=
ENST00000675979.1:c.*2452A= ENSP00000502208.1:n.*2452A=
ENST00000676044.1:c.*869A= ENSP00000502378.1:n.*869A=
ENST00000676086.1:n.4994A=
ENST00000676121.1:n.5037A=
ENST00000676237.1:c.3110A= ENSP00000501828.1:p.Glu1037=
ENST00000676416.1:c.2867A= ENSP00000501660.1:p.Glu956=
ENST00000676424.1:n.5005A=
ENST00000676429.1:n.7678A=
ENST00000374647.9:c.3209A= ENSP00000363779.5:p.Glu1070=
ENST00000467959.1:n.89A=
ENST00000495759.5:c.349A=
ENST00000537196.1:c.2162A= ENSP00000439367.1:p.Glu721=
NM_003640.3:c.3209A= , LRG_251t1:c.3209A= NP_003631.2:p.Glu1070=
XM_005252285.2:c.2867A= XP_005252342.1:p.Glu956=
XM_011519136.1:c.3209A= XP_011517438.1:p.Glu1070=
XM_011519137.1:c.2867A= XP_011517439.1:p.Glu956=
NM_001318360.1:c.2867A= NP_001305289.1:p.Glu956=
NM_001330749.1:c.2162A= NP_001317678.1:p.Glu721=
NM_003640.4:c.3209A= NP_003631.2:p.Glu1070=
XM_011519136.2:c.3209A= XP_011517438.1:p.Glu1070=
XR_929859.3:n.3598A=
NM_003640.5:c.3209A= MANE Select NP_003631.2:p.Glu1070=
NM_001318360.2:c.2867A= NP_001305289.1:p.Glu956=
NM_001330749.2:c.2162A= NP_001317678.1:p.Glu721=