Canonical Allele Identifier: CA1871337747
Gene: ELP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108900221_108900222delinsAC , CM000671.2:g.108900221_108900222delinsAC GRCh38
NC_000009.11:g.111662501_111662502delinsAC , CM000671.1:g.111662501_111662502delinsAC GRCh37
NC_000009.10:g.110702322_110702323delinsAC NCBI36
NG_008788.1:g.39107_39108delinsGT , LRG_251:g.39107_39108delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000374647.10:c.2130+38_2130+39delinsGT MANE Select ENSP00000363779.5:n.2130+38_2130+39delins...
ENST00000495759.6:c.*740+38_*740+39delinsGT ENSP00000433514.2:n.*740+38_*740+39delins...
ENST00000674535.1:c.2130+38_2130+39delinsGT ENSP00000502142.1:n.2130+38_2130+39delins...
ENST00000674704.1:n.3937+38_3937+39delinsGT
ENST00000674836.1:n.2435+38_2435+39delinsGT
ENST00000674890.1:c.2130+38_2130+39delinsGT ENSP00000501870.1:n.2130+38_2130+39delins...
ENST00000674938.1:c.1788+38_1788+39delinsGT ENSP00000502427.1:n.1788+38_1788+39delins...
ENST00000674948.1:c.1788+38_1788+39delinsGT ENSP00000501602.1:n.1788+38_1788+39delins...
ENST00000675052.1:c.2130+38_2130+39delinsGT ENSP00000502664.1:n.2130+38_2130+39delins...
ENST00000675078.1:c.2130+38_2130+39delinsGT ENSP00000501549.1:n.2130+38_2130+39delins...
ENST00000675215.1:c.*1354+38_*1354+39delinsGT ENSP00000502558.1:n.*1354+38_*1354+39deli...
ENST00000675233.1:n.3957+38_3957+39delinsGT
ENST00000675321.1:c.2130+38_2130+39delinsGT ENSP00000502751.1:n.2130+38_2130+39delins...
ENST00000675325.1:n.3926+38_3926+39delinsGT
ENST00000675335.1:c.2161+38_2161+39delinsGT ENSP00000502182.1:n.2161+38_2161+39delins...
ENST00000675400.1:n.3803+38_3803+39delinsGT
ENST00000675406.1:c.2130+38_2130+39delinsGT ENSP00000501893.1:n.2130+38_2130+39delins...
ENST00000675458.1:c.2223+38_2223+39delinsGT ENSP00000501754.1:n.2223+38_2223+39delins...
ENST00000675507.1:n.3926+38_3926+39delinsGT
ENST00000675535.1:c.2130+38_2130+39delinsGT ENSP00000501667.1:n.2130+38_2130+39delins...
ENST00000675566.1:n.3926+38_3926+39delinsGT
ENST00000675602.1:n.5178+38_5178+39delinsGT
ENST00000675647.1:n.2435+38_2435+39delinsGT
ENST00000675711.1:c.2130+38_2130+39delinsGT ENSP00000502485.1:n.2130+38_2130+39delins...
ENST00000675727.1:c.2130+38_2130+39delinsGT ENSP00000501722.1:n.2130+38_2130+39delins...
ENST00000675748.1:n.3764+38_3764+39delinsGT
ENST00000675765.1:c.2130+38_2130+39delinsGT ENSP00000502640.1:n.2130+38_2130+39delins...
ENST00000675825.1:c.2130+38_2130+39delinsGT ENSP00000502632.1:n.2130+38_2130+39delins...
ENST00000675877.1:n.2435+38_2435+39delinsGT
ENST00000675893.1:c.*3199+38_*3199+39delinsGT ENSP00000502001.1:n.*3199+38_*3199+39deli...
ENST00000675943.1:n.5745+38_5745+39delinsGT
ENST00000675979.1:c.*1373+38_*1373+39delinsGT ENSP00000502208.1:n.*1373+38_*1373+39deli...
ENST00000676044.1:c.2130+38_2130+39delinsGT ENSP00000502378.1:n.2130+38_2130+39delins...
ENST00000676086.1:n.3915+38_3915+39delinsGT
ENST00000676121.1:n.3958+38_3958+39delinsGT
ENST00000676237.1:c.2031+38_2031+39delinsGT ENSP00000501828.1:n.2031+38_2031+39delins...
ENST00000676416.1:c.1788+38_1788+39delinsGT ENSP00000501660.1:n.1788+38_1788+39delins...
ENST00000676424.1:n.3926+38_3926+39delinsGT
ENST00000676429.1:n.6599+38_6599+39delinsGT
ENST00000374647.9:c.2130+38_2130+39delinsGT ENSP00000363779.5:n.2130+38_2130+39delins...
ENST00000537196.1:c.1083+38_1083+39delinsGT ENSP00000439367.1:n.1083+38_1083+39delins...
NM_003640.3:c.2130+38_2130+39delinsGT , LRG_251t1:c.2130+38_2130+39delinsGT NP_003631.2:n.2130+38_2130+39delinsGT
XM_005252285.2:c.1788+38_1788+39delinsGT XP_005252342.1:n.1788+38_1788+39delinsGT
XM_011519136.1:c.2130+38_2130+39delinsGT XP_011517438.1:n.2130+38_2130+39delinsGT
XM_011519137.1:c.1788+38_1788+39delinsGT XP_011517439.1:n.1788+38_1788+39delinsGT
XR_929859.1:n.2446+38_2446+39delinsGT
NM_001318360.1:c.1788+38_1788+39delinsGT NP_001305289.1:n.1788+38_1788+39delinsGT
NM_001330749.1:c.1083+38_1083+39delinsGT NP_001317678.1:n.1083+38_1083+39delinsGT
NM_003640.4:c.2130+38_2130+39delinsGT NP_003631.2:n.2130+38_2130+39delinsGT
XM_011519136.2:c.2130+38_2130+39delinsGT XP_011517438.1:n.2130+38_2130+39delinsGT
XR_929859.3:n.2457+38_2457+39delinsGT
NM_003640.5:c.2130+38_2130+39delinsGT MANE Select NP_003631.2:n.2130+38_2130+39delinsGT
NM_001318360.2:c.1788+38_1788+39delinsGT NP_001305289.1:n.1788+38_1788+39delinsGT
NM_001330749.2:c.1083+38_1083+39delinsGT NP_001317678.1:n.1083+38_1083+39delinsGT