Canonical Allele Identifier: CA466673079

Gene: ELP1

Linked Data

• MyVariant Identifiers: chr9:g.111651624T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108889344T>C , CM000671.2:g.108889344T>C	GRCh38
NC_000009.11:g.111651624T>C , CM000671.1:g.111651624T>C	GRCh37
NC_000009.10:g.110691445T>C	NCBI36
NG_008788.1:g.49985A>G , LRG_251:g.49985A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000374647.10:c.3210A>G MANE Select	ENSP00000363779.5:p.Glu1070=
ENST00000495759.6:c.*1820A>G	ENSP00000433514.2:n.*1820A>G
ENST00000674535.1:c.3210A>G	ENSP00000502142.1:p.Glu1070=
ENST00000674704.1:n.6295A>G
ENST00000674836.1:n.3823A>G
ENST00000674890.1:c.*445A>G	ENSP00000501870.1:n.*445A>G
ENST00000674938.1:c.2868A>G	ENSP00000502427.1:p.Glu956=
ENST00000674948.1:c.2868A>G	ENSP00000501602.1:p.Glu956=
ENST00000675052.1:c.3210A>G	ENSP00000502664.1:p.Glu1070=
ENST00000675078.1:c.3210A>G	ENSP00000501549.1:p.Glu1070=
ENST00000675215.1:c.*2434A>G	ENSP00000502558.1:n.*2434A>G
ENST00000675233.1:n.5037A>G
ENST00000675321.1:c.3210A>G	ENSP00000502751.1:p.Glu1070=
ENST00000675325.1:n.5167A>G
ENST00000675335.1:c.3241A>G	ENSP00000502182.1:n.3241A>G
ENST00000675400.1:n.4945A>G
ENST00000675406.1:c.3210A>G	ENSP00000501893.1:p.Glu1070=
ENST00000675458.1:c.3303A>G	ENSP00000501754.1:n.3303A>G
ENST00000675507.1:n.5006A>G
ENST00000675535.1:c.*837A>G	ENSP00000501667.1:n.*837A>G
ENST00000675566.1:n.5068A>G
ENST00000675602.1:n.6258A>G
ENST00000675647.1:n.4374A>G
ENST00000675711.1:c.3210A>G	ENSP00000502485.1:p.Glu1070=
ENST00000675727.1:c.3210A>G	ENSP00000501722.1:p.Glu1070=
ENST00000675748.1:n.4844A>G
ENST00000675765.1:c.*593A>G	ENSP00000502640.1:n.*593A>G
ENST00000675825.1:c.3210A>G	ENSP00000502632.1:p.Glu1070=
ENST00000675877.1:n.3515A>G
ENST00000675893.1:c.*4279A>G	ENSP00000502001.1:n.*4279A>G
ENST00000675943.1:n.6825A>G
ENST00000675979.1:c.*2453A>G	ENSP00000502208.1:n.*2453A>G
ENST00000676044.1:c.*870A>G	ENSP00000502378.1:n.*870A>G
ENST00000676086.1:n.4995A>G
ENST00000676121.1:n.5038A>G
ENST00000676237.1:c.3111A>G	ENSP00000501828.1:p.Glu1037=
ENST00000676416.1:c.2868A>G	ENSP00000501660.1:p.Glu956=
ENST00000676424.1:n.5006A>G
ENST00000676429.1:n.7679A>G
ENST00000374647.9:c.3210A>G	ENSP00000363779.5:p.Glu1070=
ENST00000467959.1:n.90A>G
ENST00000495759.5:c.350A>G
ENST00000537196.1:c.2163A>G	ENSP00000439367.1:p.Glu721=
NM_003640.3:c.3210A>G , LRG_251t1:c.3210A>G	NP_003631.2:p.Glu1070=
XM_005252285.2:c.2868A>G	XP_005252342.1:p.Glu956=
XM_011519136.1:c.3210A>G	XP_011517438.1:p.Glu1070=
XM_011519137.1:c.2868A>G	XP_011517439.1:p.Glu956=
NM_001318360.1:c.2868A>G	NP_001305289.1:p.Glu956=
NM_001330749.1:c.2163A>G	NP_001317678.1:p.Glu721=
NM_003640.4:c.3210A>G	NP_003631.2:p.Glu1070=
XM_011519136.2:c.3210A>G	XP_011517438.1:p.Glu1070=
XR_929859.3:n.3599A>G
NM_003640.5:c.3210A>G MANE Select	NP_003631.2:p.Glu1070=
NM_001318360.2:c.2868A>G	NP_001305289.1:p.Glu956=
NM_001330749.2:c.2163A>G	NP_001317678.1:p.Glu721=