Canonical Allele Identifier: CA1871332973
Gene: ELP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108889366A= , CM000671.2:g.108889366A= GRCh38
NC_000009.11:g.111651646A= , CM000671.1:g.111651646A= GRCh37
NC_000009.10:g.110691467A= NCBI36
NG_008788.1:g.49963T= , LRG_251:g.49963T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374647.10:c.3188T= MANE Select ENSP00000363779.5:p.Ile1063=
ENST00000495759.6:c.*1798T= ENSP00000433514.2:n.*1798T=
ENST00000674535.1:c.3188T= ENSP00000502142.1:p.Ile1063=
ENST00000674704.1:n.6273T=
ENST00000674836.1:n.3801T=
ENST00000674890.1:c.*423T= ENSP00000501870.1:n.*423T=
ENST00000674938.1:c.2846T= ENSP00000502427.1:p.Ile949=
ENST00000674948.1:c.2846T= ENSP00000501602.1:p.Ile949=
ENST00000675052.1:c.3188T= ENSP00000502664.1:p.Ile1063=
ENST00000675078.1:c.3188T= ENSP00000501549.1:p.Ile1063=
ENST00000675215.1:c.*2412T= ENSP00000502558.1:n.*2412T=
ENST00000675233.1:n.5015T=
ENST00000675321.1:c.3188T= ENSP00000502751.1:p.Ile1063=
ENST00000675325.1:n.5145T=
ENST00000675335.1:c.3219T= ENSP00000502182.1:n.3219T=
ENST00000675400.1:n.4923T=
ENST00000675406.1:c.3188T= ENSP00000501893.1:p.Ile1063=
ENST00000675458.1:c.3281T= ENSP00000501754.1:n.3281T=
ENST00000675507.1:n.4984T=
ENST00000675535.1:c.*815T= ENSP00000501667.1:n.*815T=
ENST00000675566.1:n.5046T=
ENST00000675602.1:n.6236T=
ENST00000675647.1:n.4352T=
ENST00000675711.1:c.3188T= ENSP00000502485.1:p.Ile1063=
ENST00000675727.1:c.3188T= ENSP00000501722.1:p.Ile1063=
ENST00000675748.1:n.4822T=
ENST00000675765.1:c.*571T= ENSP00000502640.1:n.*571T=
ENST00000675825.1:c.3188T= ENSP00000502632.1:p.Ile1063=
ENST00000675877.1:n.3493T=
ENST00000675893.1:c.*4257T= ENSP00000502001.1:n.*4257T=
ENST00000675943.1:n.6803T=
ENST00000675979.1:c.*2431T= ENSP00000502208.1:n.*2431T=
ENST00000676044.1:c.*848T= ENSP00000502378.1:n.*848T=
ENST00000676086.1:n.4973T=
ENST00000676121.1:n.5016T=
ENST00000676237.1:c.3089T= ENSP00000501828.1:p.Ile1030=
ENST00000676416.1:c.2846T= ENSP00000501660.1:p.Ile949=
ENST00000676424.1:n.4984T=
ENST00000676429.1:n.7657T=
ENST00000374647.9:c.3188T= ENSP00000363779.5:p.Ile1063=
ENST00000467959.1:n.68T=
ENST00000495759.5:c.328T=
ENST00000537196.1:c.2141T= ENSP00000439367.1:p.Ile714=
NM_003640.3:c.3188T= , LRG_251t1:c.3188T= NP_003631.2:p.Ile1063=
XM_005252285.2:c.2846T= XP_005252342.1:p.Ile949=
XM_011519136.1:c.3188T= XP_011517438.1:p.Ile1063=
XM_011519137.1:c.2846T= XP_011517439.1:p.Ile949=
NM_001318360.1:c.2846T= NP_001305289.1:p.Ile949=
NM_001330749.1:c.2141T= NP_001317678.1:p.Ile714=
NM_003640.4:c.3188T= NP_003631.2:p.Ile1063=
XM_011519136.2:c.3188T= XP_011517438.1:p.Ile1063=
XR_929859.3:n.3577T=
NM_003640.5:c.3188T= MANE Select NP_003631.2:p.Ile1063=
NM_001318360.2:c.2846T= NP_001305289.1:p.Ile949=
NM_001330749.2:c.2141T= NP_001317678.1:p.Ile714=