Canonical Allele Identifier: CA374422915
Gene: ELP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108899822T>A , CM000671.2:g.108899822T>A GRCh38
NC_000009.11:g.111662102T>A , CM000671.1:g.111662102T>A GRCh37
NC_000009.10:g.110701923T>A NCBI36
NG_008788.1:g.39507A>T , LRG_251:g.39507A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000374647.10:c.2204A>T MANE Select ENSP00000363779.5:p.Lys735Ile
ENST00000495759.6:c.*814A>T ENSP00000433514.2:n.*814A>T
ENST00000674535.1:c.2204A>T ENSP00000502142.1:p.Lys735Ile
ENST00000674704.1:n.4011A>T
ENST00000674836.1:n.2509A>T
ENST00000674890.1:c.2204A>T ENSP00000501870.1:p.Lys735Ile
ENST00000674938.1:c.1862A>T ENSP00000502427.1:p.Lys621Ile
ENST00000674948.1:c.1862A>T ENSP00000501602.1:p.Lys621Ile
ENST00000675052.1:c.2204A>T ENSP00000502664.1:p.Lys735Ile
ENST00000675078.1:c.2204A>T ENSP00000501549.1:p.Lys735Ile
ENST00000675215.1:c.*1428A>T ENSP00000502558.1:n.*1428A>T
ENST00000675233.1:n.4031A>T
ENST00000675321.1:c.2204A>T ENSP00000502751.1:p.Lys735Ile
ENST00000675325.1:n.4000A>T
ENST00000675335.1:c.2235A>T ENSP00000502182.1:n.2235A>T
ENST00000675400.1:n.3877A>T
ENST00000675406.1:c.2204A>T ENSP00000501893.1:p.Lys735Ile
ENST00000675458.1:c.2297A>T ENSP00000501754.1:n.2297A>T
ENST00000675507.1:n.4000A>T
ENST00000675535.1:c.2204A>T ENSP00000501667.1:p.Lys735Ile
ENST00000675566.1:n.4000A>T
ENST00000675602.1:n.5252A>T
ENST00000675647.1:n.2509A>T
ENST00000675711.1:c.2204A>T ENSP00000502485.1:p.Lys735Ile
ENST00000675727.1:c.2204A>T ENSP00000501722.1:p.Lys735Ile
ENST00000675748.1:n.3838A>T
ENST00000675765.1:c.2204A>T ENSP00000502640.1:p.Lys735Ile
ENST00000675825.1:c.2204A>T ENSP00000502632.1:p.Lys735Ile
ENST00000675877.1:n.2509A>T
ENST00000675893.1:c.*3273A>T ENSP00000502001.1:n.*3273A>T
ENST00000675943.1:n.5819A>T
ENST00000675979.1:c.*1447A>T ENSP00000502208.1:n.*1447A>T
ENST00000676044.1:c.2204A>T ENSP00000502378.1:p.Lys735Ile
ENST00000676086.1:n.3989A>T
ENST00000676121.1:n.4032A>T
ENST00000676237.1:c.2105A>T ENSP00000501828.1:p.Lys702Ile
ENST00000676416.1:c.1862A>T ENSP00000501660.1:p.Lys621Ile
ENST00000676424.1:n.4000A>T
ENST00000676429.1:n.6673A>T
ENST00000374647.9:c.2204A>T ENSP00000363779.5:p.Lys735Ile
ENST00000537196.1:c.1157A>T ENSP00000439367.1:p.Lys386Ile
NM_003640.3:c.2204A>T , LRG_251t1:c.2204A>T NP_003631.2:p.Lys735Ile
XM_005252285.2:c.1862A>T XP_005252342.1:p.Lys621Ile
XM_011519136.1:c.2204A>T XP_011517438.1:p.Lys735Ile
XM_011519137.1:c.1862A>T XP_011517439.1:p.Lys621Ile
XR_929859.1:n.2520A>T
NM_001318360.1:c.1862A>T NP_001305289.1:p.Lys621Ile
NM_001330749.1:c.1157A>T NP_001317678.1:p.Lys386Ile
NM_003640.4:c.2204A>T NP_003631.2:p.Lys735Ile
XM_011519136.2:c.2204A>T XP_011517438.1:p.Lys735Ile
XR_929859.3:n.2531A>T
NM_003640.5:c.2204A>T MANE Select NP_003631.2:p.Lys735Ile
NM_001318360.2:c.1862A>T NP_001305289.1:p.Lys621Ile
NM_001330749.2:c.1157A>T NP_001317678.1:p.Lys386Ile