Canonical Allele Identifier: CA1871335005
Gene: ELP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108894009G= , CM000671.2:g.108894009G= GRCh38
NC_000009.11:g.111656289G= , CM000671.1:g.111656289G= GRCh37
NC_000009.10:g.110696110G= NCBI36
NG_008788.1:g.45320C= , LRG_251:g.45320C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374647.10:c.2794C= MANE Select ENSP00000363779.5:p.Gln932=
ENST00000495759.6:c.*1404C= ENSP00000433514.2:n.*1404C=
ENST00000674535.1:c.2794C= ENSP00000502142.1:p.Gln932=
ENST00000674704.1:n.5879C=
ENST00000674836.1:n.3407C=
ENST00000674890.1:c.*29C= ENSP00000501870.1:n.*29C=
ENST00000674938.1:c.2452C= ENSP00000502427.1:p.Gln818=
ENST00000674948.1:c.2452C= ENSP00000501602.1:p.Gln818=
ENST00000675052.1:c.2794C= ENSP00000502664.1:p.Gln932=
ENST00000675078.1:c.2794C= ENSP00000501549.1:p.Gln932=
ENST00000675215.1:c.*2018C= ENSP00000502558.1:n.*2018C=
ENST00000675233.1:n.4621C=
ENST00000675321.1:c.2794C= ENSP00000502751.1:p.Gln932=
ENST00000675325.1:n.4751C=
ENST00000675335.1:c.2825C= ENSP00000502182.1:n.2825C=
ENST00000675400.1:n.4529C=
ENST00000675406.1:c.2794C= ENSP00000501893.1:p.Gln932=
ENST00000675458.1:c.2887C= ENSP00000501754.1:n.2887C=
ENST00000675507.1:n.4590C=
ENST00000675535.1:c.*421C= ENSP00000501667.1:n.*421C=
ENST00000675566.1:n.4652C=
ENST00000675602.1:n.5842C=
ENST00000675647.1:n.3099C=
ENST00000675711.1:c.2794C= ENSP00000502485.1:p.Gln932=
ENST00000675727.1:c.2794C= ENSP00000501722.1:p.Gln932=
ENST00000675748.1:n.4428C=
ENST00000675765.1:c.*177C= ENSP00000502640.1:n.*177C=
ENST00000675825.1:c.2794C= ENSP00000502632.1:p.Gln932=
ENST00000675877.1:n.3099C=
ENST00000675893.1:c.*3863C= ENSP00000502001.1:n.*3863C=
ENST00000675943.1:n.6409C=
ENST00000675979.1:c.*2037C= ENSP00000502208.1:n.*2037C=
ENST00000676044.1:c.*454C= ENSP00000502378.1:n.*454C=
ENST00000676086.1:n.4579C=
ENST00000676121.1:n.4622C=
ENST00000676237.1:c.2695C= ENSP00000501828.1:p.Gln899=
ENST00000676416.1:c.2452C= ENSP00000501660.1:p.Gln818=
ENST00000676424.1:n.4590C=
ENST00000676429.1:n.7263C=
ENST00000374647.9:c.2794C= ENSP00000363779.5:p.Gln932=
ENST00000537196.1:c.1747C= ENSP00000439367.1:p.Gln583=
NM_003640.3:c.2794C= , LRG_251t1:c.2794C= NP_003631.2:p.Gln932=
XM_005252285.2:c.2452C= XP_005252342.1:p.Gln818=
XM_011519136.1:c.2794C= XP_011517438.1:p.Gln932=
XM_011519137.1:c.2452C= XP_011517439.1:p.Gln818=
XR_929859.1:n.3172C=
NM_001318360.1:c.2452C= NP_001305289.1:p.Gln818=
NM_001330749.1:c.1747C= NP_001317678.1:p.Gln583=
NM_003640.4:c.2794C= NP_003631.2:p.Gln932=
XM_011519136.2:c.2794C= XP_011517438.1:p.Gln932=
XR_929859.3:n.3183C=
NM_003640.5:c.2794C= MANE Select NP_003631.2:p.Gln932=
NM_001318360.2:c.2452C= NP_001305289.1:p.Gln818=
NM_001330749.2:c.1747C= NP_001317678.1:p.Gln583=