Canonical Allele Identifier: CA374414850

Gene: ELP1

Linked Data

• MyVariant Identifiers: chr9:g.111651625T>A (hg19) ; chr9:g.108889345T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108889345T>A , CM000671.2:g.108889345T>A	GRCh38
NC_000009.11:g.111651625T>A , CM000671.1:g.111651625T>A	GRCh37
NC_000009.10:g.110691446T>A	NCBI36
NG_008788.1:g.49984A>T , LRG_251:g.49984A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000374647.10:c.3209A>T MANE Select	ENSP00000363779.5:p.Glu1070Val
ENST00000495759.6:c.*1819A>T	ENSP00000433514.2:n.*1819A>T
ENST00000674535.1:c.3209A>T	ENSP00000502142.1:p.Glu1070Val
ENST00000674704.1:n.6294A>T
ENST00000674836.1:n.3822A>T
ENST00000674890.1:c.*444A>T	ENSP00000501870.1:n.*444A>T
ENST00000674938.1:c.2867A>T	ENSP00000502427.1:p.Glu956Val
ENST00000674948.1:c.2867A>T	ENSP00000501602.1:p.Glu956Val
ENST00000675052.1:c.3209A>T	ENSP00000502664.1:p.Glu1070Val
ENST00000675078.1:c.3209A>T	ENSP00000501549.1:p.Glu1070Val
ENST00000675215.1:c.*2433A>T	ENSP00000502558.1:n.*2433A>T
ENST00000675233.1:n.5036A>T
ENST00000675321.1:c.3209A>T	ENSP00000502751.1:p.Glu1070Val
ENST00000675325.1:n.5166A>T
ENST00000675335.1:c.3240A>T	ENSP00000502182.1:n.3240A>T
ENST00000675400.1:n.4944A>T
ENST00000675406.1:c.3209A>T	ENSP00000501893.1:p.Glu1070Val
ENST00000675458.1:c.3302A>T	ENSP00000501754.1:n.3302A>T
ENST00000675507.1:n.5005A>T
ENST00000675535.1:c.*836A>T	ENSP00000501667.1:n.*836A>T
ENST00000675566.1:n.5067A>T
ENST00000675602.1:n.6257A>T
ENST00000675647.1:n.4373A>T
ENST00000675711.1:c.3209A>T	ENSP00000502485.1:p.Glu1070Val
ENST00000675727.1:c.3209A>T	ENSP00000501722.1:p.Glu1070Val
ENST00000675748.1:n.4843A>T
ENST00000675765.1:c.*592A>T	ENSP00000502640.1:n.*592A>T
ENST00000675825.1:c.3209A>T	ENSP00000502632.1:p.Glu1070Val
ENST00000675877.1:n.3514A>T
ENST00000675893.1:c.*4278A>T	ENSP00000502001.1:n.*4278A>T
ENST00000675943.1:n.6824A>T
ENST00000675979.1:c.*2452A>T	ENSP00000502208.1:n.*2452A>T
ENST00000676044.1:c.*869A>T	ENSP00000502378.1:n.*869A>T
ENST00000676086.1:n.4994A>T
ENST00000676121.1:n.5037A>T
ENST00000676237.1:c.3110A>T	ENSP00000501828.1:p.Glu1037Val
ENST00000676416.1:c.2867A>T	ENSP00000501660.1:p.Glu956Val
ENST00000676424.1:n.5005A>T
ENST00000676429.1:n.7678A>T
ENST00000374647.9:c.3209A>T	ENSP00000363779.5:p.Glu1070Val
ENST00000467959.1:n.89A>T
ENST00000495759.5:c.349A>T
ENST00000537196.1:c.2162A>T	ENSP00000439367.1:p.Glu721Val
NM_003640.3:c.3209A>T , LRG_251t1:c.3209A>T	NP_003631.2:p.Glu1070Val
XM_005252285.2:c.2867A>T	XP_005252342.1:p.Glu956Val
XM_011519136.1:c.3209A>T	XP_011517438.1:p.Glu1070Val
XM_011519137.1:c.2867A>T	XP_011517439.1:p.Glu956Val
NM_001318360.1:c.2867A>T	NP_001305289.1:p.Glu956Val
NM_001330749.1:c.2162A>T	NP_001317678.1:p.Glu721Val
NM_003640.4:c.3209A>T	NP_003631.2:p.Glu1070Val
XM_011519136.2:c.3209A>T	XP_011517438.1:p.Glu1070Val
XR_929859.3:n.3598A>T
NM_003640.5:c.3209A>T MANE Select	NP_003631.2:p.Glu1070Val
NM_001318360.2:c.2867A>T	NP_001305289.1:p.Glu956Val
NM_001330749.2:c.2162A>T	NP_001317678.1:p.Glu721Val