Canonical Allele Identifier: CA1871337748
Gene: ELP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108900221_108900225delinsACAAT , CM000671.2:g.108900221_108900225delinsACAAT GRCh38
NC_000009.11:g.111662501_111662505delinsACAAT , CM000671.1:g.111662501_111662505delinsACAAT GRCh37
NC_000009.10:g.110702322_110702326delinsACAAT NCBI36
NG_008788.1:g.39104_39108delinsATTGT , LRG_251:g.39104_39108delinsATTGT

Transcript Alleles

HGVS Amino-acid change
ENST00000374647.10:c.2130+35_2130+39delinsATTGT MANE Select ENSP00000363779.5:n.2130+35_2130+39delins...
ENST00000495759.6:c.*740+35_*740+39delinsATTGT ENSP00000433514.2:n.*740+35_*740+39delins...
ENST00000674535.1:c.2130+35_2130+39delinsATTGT ENSP00000502142.1:n.2130+35_2130+39delins...
ENST00000674704.1:n.3937+35_3937+39delinsATTGT
ENST00000674836.1:n.2435+35_2435+39delinsATTGT
ENST00000674890.1:c.2130+35_2130+39delinsATTGT ENSP00000501870.1:n.2130+35_2130+39delins...
ENST00000674938.1:c.1788+35_1788+39delinsATTGT ENSP00000502427.1:n.1788+35_1788+39delins...
ENST00000674948.1:c.1788+35_1788+39delinsATTGT ENSP00000501602.1:n.1788+35_1788+39delins...
ENST00000675052.1:c.2130+35_2130+39delinsATTGT ENSP00000502664.1:n.2130+35_2130+39delins...
ENST00000675078.1:c.2130+35_2130+39delinsATTGT ENSP00000501549.1:n.2130+35_2130+39delins...
ENST00000675215.1:c.*1354+35_*1354+39delinsATTGT ENSP00000502558.1:n.*1354+35_*1354+39deli...
ENST00000675233.1:n.3957+35_3957+39delinsATTGT
ENST00000675321.1:c.2130+35_2130+39delinsATTGT ENSP00000502751.1:n.2130+35_2130+39delins...
ENST00000675325.1:n.3926+35_3926+39delinsATTGT
ENST00000675335.1:c.2161+35_2161+39delinsATTGT ENSP00000502182.1:n.2161+35_2161+39delins...
ENST00000675400.1:n.3803+35_3803+39delinsATTGT
ENST00000675406.1:c.2130+35_2130+39delinsATTGT ENSP00000501893.1:n.2130+35_2130+39delins...
ENST00000675458.1:c.2223+35_2223+39delinsATTGT ENSP00000501754.1:n.2223+35_2223+39delins...
ENST00000675507.1:n.3926+35_3926+39delinsATTGT
ENST00000675535.1:c.2130+35_2130+39delinsATTGT ENSP00000501667.1:n.2130+35_2130+39delins...
ENST00000675566.1:n.3926+35_3926+39delinsATTGT
ENST00000675602.1:n.5178+35_5178+39delinsATTGT
ENST00000675647.1:n.2435+35_2435+39delinsATTGT
ENST00000675711.1:c.2130+35_2130+39delinsATTGT ENSP00000502485.1:n.2130+35_2130+39delins...
ENST00000675727.1:c.2130+35_2130+39delinsATTGT ENSP00000501722.1:n.2130+35_2130+39delins...
ENST00000675748.1:n.3764+35_3764+39delinsATTGT
ENST00000675765.1:c.2130+35_2130+39delinsATTGT ENSP00000502640.1:n.2130+35_2130+39delins...
ENST00000675825.1:c.2130+35_2130+39delinsATTGT ENSP00000502632.1:n.2130+35_2130+39delins...
ENST00000675877.1:n.2435+35_2435+39delinsATTGT
ENST00000675893.1:c.*3199+35_*3199+39delinsATTGT ENSP00000502001.1:n.*3199+35_*3199+39deli...
ENST00000675943.1:n.5745+35_5745+39delinsATTGT
ENST00000675979.1:c.*1373+35_*1373+39delinsATTGT ENSP00000502208.1:n.*1373+35_*1373+39deli...
ENST00000676044.1:c.2130+35_2130+39delinsATTGT ENSP00000502378.1:n.2130+35_2130+39delins...
ENST00000676086.1:n.3915+35_3915+39delinsATTGT
ENST00000676121.1:n.3958+35_3958+39delinsATTGT
ENST00000676237.1:c.2031+35_2031+39delinsATTGT ENSP00000501828.1:n.2031+35_2031+39delins...
ENST00000676416.1:c.1788+35_1788+39delinsATTGT ENSP00000501660.1:n.1788+35_1788+39delins...
ENST00000676424.1:n.3926+35_3926+39delinsATTGT
ENST00000676429.1:n.6599+35_6599+39delinsATTGT
ENST00000374647.9:c.2130+35_2130+39delinsATTGT ENSP00000363779.5:n.2130+35_2130+39delins...
ENST00000537196.1:c.1083+35_1083+39delinsATTGT ENSP00000439367.1:n.1083+35_1083+39delins...
NM_003640.3:c.2130+35_2130+39delinsATTGT , LRG_251t1:c.2130+35_2130+39delinsATTGT NP_003631.2:n.2130+35_2130+39delinsATTGT
XM_005252285.2:c.1788+35_1788+39delinsATTGT XP_005252342.1:n.1788+35_1788+39delinsATT...
XM_011519136.1:c.2130+35_2130+39delinsATTGT XP_011517438.1:n.2130+35_2130+39delinsATT...
XM_011519137.1:c.1788+35_1788+39delinsATTGT XP_011517439.1:n.1788+35_1788+39delinsATT...
XR_929859.1:n.2446+35_2446+39delinsATTGT
NM_001318360.1:c.1788+35_1788+39delinsATTGT NP_001305289.1:n.1788+35_1788+39delinsATT...
NM_001330749.1:c.1083+35_1083+39delinsATTGT NP_001317678.1:n.1083+35_1083+39delinsATT...
NM_003640.4:c.2130+35_2130+39delinsATTGT NP_003631.2:n.2130+35_2130+39delinsATTGT
XM_011519136.2:c.2130+35_2130+39delinsATTGT XP_011517438.1:n.2130+35_2130+39delinsATT...
XR_929859.3:n.2457+35_2457+39delinsATTGT
NM_003640.5:c.2130+35_2130+39delinsATTGT MANE Select NP_003631.2:n.2130+35_2130+39delinsATTGT
NM_001318360.2:c.1788+35_1788+39delinsATTGT NP_001305289.1:n.1788+35_1788+39delinsATT...
NM_001330749.2:c.1083+35_1083+39delinsATTGT NP_001317678.1:n.1083+35_1083+39delinsATT...