Canonical Allele Identifier: CA2691095750
Gene: ELP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108899684_108899688del , CM000671.2:g.108899684_108899688del GRCh38
NC_000009.11:g.111661964_111661968del , CM000671.1:g.111661964_111661968del GRCh37
NC_000009.10:g.110701785_110701789del NCBI36
NG_008788.1:g.39641_39645del , LRG_251:g.39641_39645del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374647.10:c.2204+134_2204+138del MANE Select ENSP00000363779.5:n.2204+134_2204+138del
ENST00000495759.6:c.*814+134_*814+138del ENSP00000433514.2:n.*814+134_*814+138del
ENST00000674535.1:c.2204+134_2204+138del ENSP00000502142.1:n.2204+134_2204+138del
ENST00000674704.1:n.4011+134_4011+138del
ENST00000674836.1:n.2509+134_2509+138del
ENST00000674890.1:c.2204+134_2204+138del ENSP00000501870.1:n.2204+134_2204+138del
ENST00000674938.1:c.1862+134_1862+138del ENSP00000502427.1:n.1862+134_1862+138del
ENST00000674948.1:c.1862+134_1862+138del ENSP00000501602.1:n.1862+134_1862+138del
ENST00000675052.1:c.2204+134_2204+138del ENSP00000502664.1:n.2204+134_2204+138del
ENST00000675078.1:c.2204+134_2204+138del ENSP00000501549.1:n.2204+134_2204+138del
ENST00000675215.1:c.*1428+134_*1428+138del ENSP00000502558.1:n.*1428+134_*1428+138del
ENST00000675233.1:n.4031+134_4031+138del
ENST00000675321.1:c.2204+134_2204+138del ENSP00000502751.1:n.2204+134_2204+138del
ENST00000675325.1:n.4000+134_4000+138del
ENST00000675335.1:c.2235+134_2235+138del ENSP00000502182.1:n.2235+134_2235+138del
ENST00000675400.1:n.3877+134_3877+138del
ENST00000675406.1:c.2204+134_2204+138del ENSP00000501893.1:n.2204+134_2204+138del
ENST00000675458.1:c.2297+134_2297+138del ENSP00000501754.1:n.2297+134_2297+138del
ENST00000675507.1:n.4000+134_4000+138del
ENST00000675535.1:c.2204+134_2204+138del ENSP00000501667.1:n.2204+134_2204+138del
ENST00000675566.1:n.4000+134_4000+138del
ENST00000675602.1:n.5252+134_5252+138del
ENST00000675647.1:n.2509+134_2509+138del
ENST00000675711.1:c.2204+134_2204+138del ENSP00000502485.1:n.2204+134_2204+138del
ENST00000675727.1:c.2204+134_2204+138del ENSP00000501722.1:n.2204+134_2204+138del
ENST00000675748.1:n.3838+134_3838+138del
ENST00000675765.1:c.2204+134_2204+138del ENSP00000502640.1:n.2204+134_2204+138del
ENST00000675825.1:c.2204+134_2204+138del ENSP00000502632.1:n.2204+134_2204+138del
ENST00000675877.1:n.2509+134_2509+138del
ENST00000675893.1:c.*3273+134_*3273+138del ENSP00000502001.1:n.*3273+134_*3273+138del
ENST00000675943.1:n.5819+134_5819+138del
ENST00000675979.1:c.*1447+134_*1447+138del ENSP00000502208.1:n.*1447+134_*1447+138del
ENST00000676044.1:c.2204+134_2204+138del ENSP00000502378.1:n.2204+134_2204+138del
ENST00000676086.1:n.3989+134_3989+138del
ENST00000676121.1:n.4032+134_4032+138del
ENST00000676237.1:c.2105+134_2105+138del ENSP00000501828.1:n.2105+134_2105+138del
ENST00000676416.1:c.1862+134_1862+138del ENSP00000501660.1:n.1862+134_1862+138del
ENST00000676424.1:n.4000+134_4000+138del
ENST00000676429.1:n.6673+134_6673+138del
ENST00000374647.9:c.2204+134_2204+138del ENSP00000363779.5:n.2204+134_2204+138del
ENST00000537196.1:c.1157+134_1157+138del ENSP00000439367.1:n.1157+134_1157+138del
NM_003640.3:c.2204+134_2204+138del , LRG_251t1:c.2204+134_2204+138del NP_003631.2:n.2204+134_2204+138del
XM_005252285.2:c.1862+134_1862+138del XP_005252342.1:n.1862+134_1862+138del
XM_011519136.1:c.2204+134_2204+138del XP_011517438.1:n.2204+134_2204+138del
XM_011519137.1:c.1862+134_1862+138del XP_011517439.1:n.1862+134_1862+138del
XR_929859.1:n.2520+134_2520+138del
NM_001318360.1:c.1862+134_1862+138del NP_001305289.1:n.1862+134_1862+138del
NM_001330749.1:c.1157+134_1157+138del NP_001317678.1:n.1157+134_1157+138del
NM_003640.4:c.2204+134_2204+138del NP_003631.2:n.2204+134_2204+138del
XM_011519136.2:c.2204+134_2204+138del XP_011517438.1:n.2204+134_2204+138del
XR_929859.3:n.2531+134_2531+138del
NM_003640.5:c.2204+134_2204+138del MANE Select NP_003631.2:n.2204+134_2204+138del
NM_001318360.2:c.1862+134_1862+138del NP_001305289.1:n.1862+134_1862+138del
NM_001330749.2:c.1157+134_1157+138del NP_001317678.1:n.1157+134_1157+138del