Canonical Allele Identifier: CA1871332983
Gene: ELP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108889410C= , CM000671.2:g.108889410C= GRCh38
NC_000009.11:g.111651690C= , CM000671.1:g.111651690C= GRCh37
NC_000009.10:g.110691511C= NCBI36
NG_008788.1:g.49919G= , LRG_251:g.49919G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374647.10:c.3161-17G= MANE Select ENSP00000363779.5:n.3161-17G=
ENST00000495759.6:c.*1771-17G= ENSP00000433514.2:n.*1771-17G=
ENST00000674535.1:c.3161-17G= ENSP00000502142.1:n.3161-17G=
ENST00000674704.1:n.6246-17G=
ENST00000674836.1:n.3774-17G=
ENST00000674890.1:c.*396-17G= ENSP00000501870.1:n.*396-17G=
ENST00000674938.1:c.2819-17G= ENSP00000502427.1:n.2819-17G=
ENST00000674948.1:c.2819-17G= ENSP00000501602.1:n.2819-17G=
ENST00000675052.1:c.3161-17G= ENSP00000502664.1:n.3161-17G=
ENST00000675078.1:c.3161-17G= ENSP00000501549.1:n.3161-17G=
ENST00000675215.1:c.*2385-17G= ENSP00000502558.1:n.*2385-17G=
ENST00000675233.1:n.4988-17G=
ENST00000675321.1:c.3161-17G= ENSP00000502751.1:n.3161-17G=
ENST00000675325.1:n.5118-17G=
ENST00000675335.1:c.3192-17G= ENSP00000502182.1:n.3192-17G=
ENST00000675400.1:n.4896-17G=
ENST00000675406.1:c.3161-17G= ENSP00000501893.1:n.3161-17G=
ENST00000675458.1:c.3254-17G= ENSP00000501754.1:n.3254-17G=
ENST00000675507.1:n.4957-17G=
ENST00000675535.1:c.*788-17G= ENSP00000501667.1:n.*788-17G=
ENST00000675566.1:n.5019-17G=
ENST00000675602.1:n.6209-17G=
ENST00000675647.1:n.4325-17G=
ENST00000675711.1:c.3161-17G= ENSP00000502485.1:n.3161-17G=
ENST00000675727.1:c.3161-17G= ENSP00000501722.1:n.3161-17G=
ENST00000675748.1:n.4795-17G=
ENST00000675765.1:c.*544-17G= ENSP00000502640.1:n.*544-17G=
ENST00000675825.1:c.3161-17G= ENSP00000502632.1:n.3161-17G=
ENST00000675877.1:n.3466-17G=
ENST00000675893.1:c.*4230-17G= ENSP00000502001.1:n.*4230-17G=
ENST00000675943.1:n.6776-17G=
ENST00000675979.1:c.*2404-17G= ENSP00000502208.1:n.*2404-17G=
ENST00000676044.1:c.*821-17G= ENSP00000502378.1:n.*821-17G=
ENST00000676086.1:n.4946-17G=
ENST00000676121.1:n.4989-17G=
ENST00000676237.1:c.3062-17G= ENSP00000501828.1:n.3062-17G=
ENST00000676416.1:c.2819-17G= ENSP00000501660.1:n.2819-17G=
ENST00000676424.1:n.4957-17G=
ENST00000676429.1:n.7630-17G=
ENST00000374647.9:c.3161-17G= ENSP00000363779.5:n.3161-17G=
ENST00000467959.1:n.41-17G=
ENST00000495759.5:c.301-17G=
ENST00000537196.1:c.2114-17G= ENSP00000439367.1:n.2114-17G=
NM_003640.3:c.3161-17G= , LRG_251t1:c.3161-17G= NP_003631.2:n.3161-17G=
XM_005252285.2:c.2819-17G= XP_005252342.1:n.2819-17G=
XM_011519136.1:c.3161-17G= XP_011517438.1:n.3161-17G=
XM_011519137.1:c.2819-17G= XP_011517439.1:n.2819-17G=
NM_001318360.1:c.2819-17G= NP_001305289.1:n.2819-17G=
NM_001330749.1:c.2114-17G= NP_001317678.1:n.2114-17G=
NM_003640.4:c.3161-17G= NP_003631.2:n.3161-17G=
XM_011519136.2:c.3161-17G= XP_011517438.1:n.3161-17G=
XR_929859.3:n.3550-17G=
NM_003640.5:c.3161-17G= MANE Select NP_003631.2:n.3161-17G=
NM_001318360.2:c.2819-17G= NP_001305289.1:n.2819-17G=
NM_001330749.2:c.2114-17G= NP_001317678.1:n.2114-17G=