Canonical Allele Identifier: CA466673549

Gene: ELP1

Linked Data

• MyVariant Identifiers: chr9:g.111656278A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108893998A>T , CM000671.2:g.108893998A>T	GRCh38
NC_000009.11:g.111656278A>T , CM000671.1:g.111656278A>T	GRCh37
NC_000009.10:g.110696099A>T	NCBI36
NG_008788.1:g.45331T>A , LRG_251:g.45331T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000374647.10:c.2805T>A MANE Select	ENSP00000363779.5:p.Thr935=
ENST00000495759.6:c.*1415T>A	ENSP00000433514.2:n.*1415T>A
ENST00000674535.1:c.2805T>A	ENSP00000502142.1:p.Thr935=
ENST00000674704.1:n.5890T>A
ENST00000674836.1:n.3418T>A
ENST00000674890.1:c.*40T>A	ENSP00000501870.1:n.*40T>A
ENST00000674938.1:c.2463T>A	ENSP00000502427.1:p.Thr821=
ENST00000674948.1:c.2463T>A	ENSP00000501602.1:p.Thr821=
ENST00000675052.1:c.2805T>A	ENSP00000502664.1:p.Thr935=
ENST00000675078.1:c.2805T>A	ENSP00000501549.1:p.Thr935=
ENST00000675215.1:c.*2029T>A	ENSP00000502558.1:n.*2029T>A
ENST00000675233.1:n.4632T>A
ENST00000675321.1:c.2805T>A	ENSP00000502751.1:p.Thr935=
ENST00000675325.1:n.4762T>A
ENST00000675335.1:c.2836T>A	ENSP00000502182.1:n.2836T>A
ENST00000675400.1:n.4540T>A
ENST00000675406.1:c.2805T>A	ENSP00000501893.1:p.Thr935=
ENST00000675458.1:c.2898T>A	ENSP00000501754.1:n.2898T>A
ENST00000675507.1:n.4601T>A
ENST00000675535.1:c.*432T>A	ENSP00000501667.1:n.*432T>A
ENST00000675566.1:n.4663T>A
ENST00000675602.1:n.5853T>A
ENST00000675647.1:n.3110T>A
ENST00000675711.1:c.2805T>A	ENSP00000502485.1:p.Thr935=
ENST00000675727.1:c.2805T>A	ENSP00000501722.1:p.Thr935=
ENST00000675748.1:n.4439T>A
ENST00000675765.1:c.*188T>A	ENSP00000502640.1:n.*188T>A
ENST00000675825.1:c.2805T>A	ENSP00000502632.1:p.Thr935=
ENST00000675877.1:n.3110T>A
ENST00000675893.1:c.*3874T>A	ENSP00000502001.1:n.*3874T>A
ENST00000675943.1:n.6420T>A
ENST00000675979.1:c.*2048T>A	ENSP00000502208.1:n.*2048T>A
ENST00000676044.1:c.*465T>A	ENSP00000502378.1:n.*465T>A
ENST00000676086.1:n.4590T>A
ENST00000676121.1:n.4633T>A
ENST00000676237.1:c.2706T>A	ENSP00000501828.1:p.Thr902=
ENST00000676416.1:c.2463T>A	ENSP00000501660.1:p.Thr821=
ENST00000676424.1:n.4601T>A
ENST00000676429.1:n.7274T>A
ENST00000374647.9:c.2805T>A	ENSP00000363779.5:p.Thr935=
ENST00000537196.1:c.1758T>A	ENSP00000439367.1:p.Thr586=
NM_003640.3:c.2805T>A , LRG_251t1:c.2805T>A	NP_003631.2:p.Thr935=
XM_005252285.2:c.2463T>A	XP_005252342.1:p.Thr821=
XM_011519136.1:c.2805T>A	XP_011517438.1:p.Thr935=
XM_011519137.1:c.2463T>A	XP_011517439.1:p.Thr821=
XR_929859.1:n.3183T>A
NM_001318360.1:c.2463T>A	NP_001305289.1:p.Thr821=
NM_001330749.1:c.1758T>A	NP_001317678.1:p.Thr586=
NM_003640.4:c.2805T>A	NP_003631.2:p.Thr935=
XM_011519136.2:c.2805T>A	XP_011517438.1:p.Thr935=
XR_929859.3:n.3194T>A
NM_003640.5:c.2805T>A MANE Select	NP_003631.2:p.Thr935=
NM_001318360.2:c.2463T>A	NP_001305289.1:p.Thr821=
NM_001330749.2:c.1758T>A	NP_001317678.1:p.Thr586=