Canonical Allele Identifier: CA5174539

Gene: ELP1

Linked Data

• dbSNP Id: rs766689615
• ExAC: 9:111656289 G / A
• gnomAD v2: 9-111656289-G-A
• gnomAD v3: 9-108894009-G-A
• gnomAD v4: 9-108894009-G-A
• MyVariant Identifiers: chr9:g.111656289G>A (hg19) ; chr9:g.108894009G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108894009G>A , CM000671.2:g.108894009G>A	GRCh38
NC_000009.11:g.111656289G>A , CM000671.1:g.111656289G>A	GRCh37
NC_000009.10:g.110696110G>A	NCBI36
NG_008788.1:g.45320C>T , LRG_251:g.45320C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000374647.10:c.2794C>T MANE Select	ENSP00000363779.5:p.Gln932Ter
ENST00000495759.6:c.*1404C>T	ENSP00000433514.2:n.*1404C>T
ENST00000674535.1:c.2794C>T	ENSP00000502142.1:p.Gln932Ter
ENST00000674704.1:n.5879C>T
ENST00000674836.1:n.3407C>T
ENST00000674890.1:c.*29C>T	ENSP00000501870.1:n.*29C>T
ENST00000674938.1:c.2452C>T	ENSP00000502427.1:p.Gln818Ter
ENST00000674948.1:c.2452C>T	ENSP00000501602.1:p.Gln818Ter
ENST00000675052.1:c.2794C>T	ENSP00000502664.1:p.Gln932Ter
ENST00000675078.1:c.2794C>T	ENSP00000501549.1:p.Gln932Ter
ENST00000675215.1:c.*2018C>T	ENSP00000502558.1:n.*2018C>T
ENST00000675233.1:n.4621C>T
ENST00000675321.1:c.2794C>T	ENSP00000502751.1:p.Gln932Ter
ENST00000675325.1:n.4751C>T
ENST00000675335.1:c.2825C>T	ENSP00000502182.1:n.2825C>T
ENST00000675400.1:n.4529C>T
ENST00000675406.1:c.2794C>T	ENSP00000501893.1:p.Gln932Ter
ENST00000675458.1:c.2887C>T	ENSP00000501754.1:n.2887C>T
ENST00000675507.1:n.4590C>T
ENST00000675535.1:c.*421C>T	ENSP00000501667.1:n.*421C>T
ENST00000675566.1:n.4652C>T
ENST00000675602.1:n.5842C>T
ENST00000675647.1:n.3099C>T
ENST00000675711.1:c.2794C>T	ENSP00000502485.1:p.Gln932Ter
ENST00000675727.1:c.2794C>T	ENSP00000501722.1:p.Gln932Ter
ENST00000675748.1:n.4428C>T
ENST00000675765.1:c.*177C>T	ENSP00000502640.1:n.*177C>T
ENST00000675825.1:c.2794C>T	ENSP00000502632.1:p.Gln932Ter
ENST00000675877.1:n.3099C>T
ENST00000675893.1:c.*3863C>T	ENSP00000502001.1:n.*3863C>T
ENST00000675943.1:n.6409C>T
ENST00000675979.1:c.*2037C>T	ENSP00000502208.1:n.*2037C>T
ENST00000676044.1:c.*454C>T	ENSP00000502378.1:n.*454C>T
ENST00000676086.1:n.4579C>T
ENST00000676121.1:n.4622C>T
ENST00000676237.1:c.2695C>T	ENSP00000501828.1:p.Gln899Ter
ENST00000676416.1:c.2452C>T	ENSP00000501660.1:p.Gln818Ter
ENST00000676424.1:n.4590C>T
ENST00000676429.1:n.7263C>T
ENST00000374647.9:c.2794C>T	ENSP00000363779.5:p.Gln932Ter
ENST00000537196.1:c.1747C>T	ENSP00000439367.1:p.Gln583Ter
NM_003640.3:c.2794C>T , LRG_251t1:c.2794C>T	NP_003631.2:p.Gln932Ter
XM_005252285.2:c.2452C>T	XP_005252342.1:p.Gln818Ter
XM_011519136.1:c.2794C>T	XP_011517438.1:p.Gln932Ter
XM_011519137.1:c.2452C>T	XP_011517439.1:p.Gln818Ter
XR_929859.1:n.3172C>T
NM_001318360.1:c.2452C>T	NP_001305289.1:p.Gln818Ter
NM_001330749.1:c.1747C>T	NP_001317678.1:p.Gln583Ter
NM_003640.4:c.2794C>T	NP_003631.2:p.Gln932Ter
XM_011519136.2:c.2794C>T	XP_011517438.1:p.Gln932Ter
XR_929859.3:n.3183C>T
NM_003640.5:c.2794C>T MANE Select	NP_003631.2:p.Gln932Ter
NM_001318360.2:c.2452C>T	NP_001305289.1:p.Gln818Ter
NM_001330749.2:c.1747C>T	NP_001317678.1:p.Gln583Ter