Canonical Allele Identifier: CA5174535

Gene: ELP1

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108894004C>T , CM000671.2:g.108894004C>T	GRCh38
NC_000009.11:g.111656284C>T , CM000671.1:g.111656284C>T	GRCh37
NC_000009.10:g.110696105C>T	NCBI36
NG_008788.1:g.45325G>A , LRG_251:g.45325G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374647.10:c.2799G>A MANE Select	ENSP00000363779.5:p.Arg933=
ENST00000495759.6:c.*1409G>A	ENSP00000433514.2:n.*1409G>A
ENST00000674535.1:c.2799G>A	ENSP00000502142.1:p.Arg933=
ENST00000674704.1:n.5884G>A
ENST00000674836.1:n.3412G>A
ENST00000674890.1:c.*34G>A	ENSP00000501870.1:n.*34G>A
ENST00000674938.1:c.2457G>A	ENSP00000502427.1:p.Arg819=
ENST00000674948.1:c.2457G>A	ENSP00000501602.1:p.Arg819=
ENST00000675052.1:c.2799G>A	ENSP00000502664.1:p.Arg933=
ENST00000675078.1:c.2799G>A	ENSP00000501549.1:p.Arg933=
ENST00000675215.1:c.*2023G>A	ENSP00000502558.1:n.*2023G>A
ENST00000675233.1:n.4626G>A
ENST00000675321.1:c.2799G>A	ENSP00000502751.1:p.Arg933=
ENST00000675325.1:n.4756G>A
ENST00000675335.1:c.2830G>A	ENSP00000502182.1:n.2830G>A
ENST00000675400.1:n.4534G>A
ENST00000675406.1:c.2799G>A	ENSP00000501893.1:p.Arg933=
ENST00000675458.1:c.2892G>A	ENSP00000501754.1:n.2892G>A
ENST00000675507.1:n.4595G>A
ENST00000675535.1:c.*426G>A	ENSP00000501667.1:n.*426G>A
ENST00000675566.1:n.4657G>A
ENST00000675602.1:n.5847G>A
ENST00000675647.1:n.3104G>A
ENST00000675711.1:c.2799G>A	ENSP00000502485.1:p.Arg933=
ENST00000675727.1:c.2799G>A	ENSP00000501722.1:p.Arg933=
ENST00000675748.1:n.4433G>A
ENST00000675765.1:c.*182G>A	ENSP00000502640.1:n.*182G>A
ENST00000675825.1:c.2799G>A	ENSP00000502632.1:p.Arg933=
ENST00000675877.1:n.3104G>A
ENST00000675893.1:c.*3868G>A	ENSP00000502001.1:n.*3868G>A
ENST00000675943.1:n.6414G>A
ENST00000675979.1:c.*2042G>A	ENSP00000502208.1:n.*2042G>A
ENST00000676044.1:c.*459G>A	ENSP00000502378.1:n.*459G>A
ENST00000676086.1:n.4584G>A
ENST00000676121.1:n.4627G>A
ENST00000676237.1:c.2700G>A	ENSP00000501828.1:p.Arg900=
ENST00000676416.1:c.2457G>A	ENSP00000501660.1:p.Arg819=
ENST00000676424.1:n.4595G>A
ENST00000676429.1:n.7268G>A
ENST00000374647.9:c.2799G>A	ENSP00000363779.5:p.Arg933=
ENST00000537196.1:c.1752G>A	ENSP00000439367.1:p.Arg584=
NM_003640.3:c.2799G>A , LRG_251t1:c.2799G>A	NP_003631.2:p.Arg933=
XM_005252285.2:c.2457G>A	XP_005252342.1:p.Arg819=
XM_011519136.1:c.2799G>A	XP_011517438.1:p.Arg933=
XM_011519137.1:c.2457G>A	XP_011517439.1:p.Arg819=
XR_929859.1:n.3177G>A
NM_001318360.1:c.2457G>A	NP_001305289.1:p.Arg819=
NM_001330749.1:c.1752G>A	NP_001317678.1:p.Arg584=
NM_003640.4:c.2799G>A	NP_003631.2:p.Arg933=
XM_011519136.2:c.2799G>A	XP_011517438.1:p.Arg933=
XR_929859.3:n.3188G>A
NM_003640.5:c.2799G>A MANE Select	NP_003631.2:p.Arg933=
NM_001318360.2:c.2457G>A	NP_001305289.1:p.Arg819=
NM_001330749.2:c.1752G>A	NP_001317678.1:p.Arg584=