Canonical Allele Identifier: CA1871346069
Gene: ELP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108917858G= , CM000671.2:g.108917858G= GRCh38
NC_000009.11:g.111680138G= , CM000671.1:g.111680138G= GRCh37
NC_000009.10:g.110719959G= NCBI36
NG_008788.1:g.21471C= , LRG_251:g.21471C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374647.10:c.741-188C= MANE Select ENSP00000363779.5:n.741-188C=
ENST00000495759.6:c.552+4984C= ENSP00000433514.2:n.552+4984C=
ENST00000674535.1:c.741-188C= ENSP00000502142.1:n.741-188C=
ENST00000674704.1:n.2360C=
ENST00000674836.1:n.1046-188C=
ENST00000674890.1:c.741-188C= ENSP00000501870.1:n.741-188C=
ENST00000674938.1:c.399-188C= ENSP00000502427.1:n.399-188C=
ENST00000674948.1:c.399-188C= ENSP00000501602.1:n.399-188C=
ENST00000675052.1:c.741-188C= ENSP00000502664.1:n.741-188C=
ENST00000675078.1:c.741-188C= ENSP00000501549.1:n.741-188C=
ENST00000675215.1:c.553-188C= ENSP00000502558.1:n.553-188C=
ENST00000675233.1:n.2349C=
ENST00000675321.1:c.741-188C= ENSP00000502751.1:n.741-188C=
ENST00000675325.1:n.2349C=
ENST00000675335.1:c.741-188C= ENSP00000502182.1:n.741-188C=
ENST00000675400.1:n.2226C=
ENST00000675406.1:c.741-188C= ENSP00000501893.1:n.741-188C=
ENST00000675458.1:c.834-188C= ENSP00000501754.1:n.834-188C=
ENST00000675507.1:n.2349C=
ENST00000675535.1:c.741-188C= ENSP00000501667.1:n.741-188C=
ENST00000675566.1:n.2349C=
ENST00000675602.1:n.2352C=
ENST00000675647.1:n.1046-188C=
ENST00000675711.1:c.741-188C= ENSP00000502485.1:n.741-188C=
ENST00000675727.1:c.741-188C= ENSP00000501722.1:n.741-188C=
ENST00000675748.1:n.2187C=
ENST00000675765.1:c.741-188C= ENSP00000502640.1:n.741-188C=
ENST00000675825.1:c.741-188C= ENSP00000502632.1:n.741-188C=
ENST00000675877.1:n.1046-188C=
ENST00000675893.1:c.*1622C= ENSP00000502001.1:n.*1622C=
ENST00000675943.1:n.2349C=
ENST00000675979.1:c.650-188C= ENSP00000502208.1:n.650-188C=
ENST00000676044.1:c.741-188C= ENSP00000502378.1:n.741-188C=
ENST00000676086.1:n.2349C=
ENST00000676121.1:n.2381C=
ENST00000676237.1:c.650-196C= ENSP00000501828.1:n.650-196C=
ENST00000676416.1:c.399-188C= ENSP00000501660.1:n.399-188C=
ENST00000676424.1:n.2349C=
ENST00000676429.1:n.5022C=
ENST00000374647.9:c.741-188C= ENSP00000363779.5:n.741-188C=
ENST00000537196.1:c.-307-188C= ENSP00000439367.1:n.-307-188C=
NM_003640.3:c.741-188C= , LRG_251t1:c.741-188C= NP_003631.2:n.741-188C=
XM_005252285.2:c.399-188C= XP_005252342.1:n.399-188C=
XM_011519136.1:c.741-188C= XP_011517438.1:n.741-188C=
XM_011519137.1:c.399-188C= XP_011517439.1:n.399-188C=
XR_929859.1:n.1057-188C=
NM_001318360.1:c.399-188C= NP_001305289.1:n.399-188C=
NM_001330749.1:c.-307-188C= NP_001317678.1:n.-307-188C=
NM_003640.4:c.741-188C= NP_003631.2:n.741-188C=
XM_011519136.2:c.741-188C= XP_011517438.1:n.741-188C=
XR_929859.3:n.1068-188C=
NM_003640.5:c.741-188C= MANE Select NP_003631.2:n.741-188C=
NM_001318360.2:c.399-188C= NP_001305289.1:n.399-188C=
NM_001330749.2:c.-307-188C= NP_001317678.1:n.-307-188C=