Canonical Allele Identifier: CA374411989

Gene: ELP1

Linked Data

• MyVariant Identifiers: chr9:g.111641831T>A (hg19) ; chr9:g.108879551T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108879551T>A , CM000671.2:g.108879551T>A	GRCh38
NC_000009.11:g.111641831T>A , CM000671.1:g.111641831T>A	GRCh37
NC_000009.10:g.110681652T>A	NCBI36
NG_008788.1:g.59778A>T , LRG_251:g.59778A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000374647.10:c.3467A>T MANE Select	ENSP00000363779.5:p.Glu1156Val
ENST00000495759.6:c.*2077A>T	ENSP00000433514.2:n.*2077A>T
ENST00000674535.1:c.3467A>T	ENSP00000502142.1:p.Glu1156Val
ENST00000674704.1:n.6552A>T
ENST00000674740.1:n.350A>T
ENST00000674836.1:n.4080A>T
ENST00000674890.1:c.*702A>T	ENSP00000501870.1:n.*702A>T
ENST00000674938.1:c.3125A>T	ENSP00000502427.1:p.Glu1042Val
ENST00000674948.1:c.3125A>T	ENSP00000501602.1:p.Glu1042Val
ENST00000675052.1:c.3467A>T	ENSP00000502664.1:p.Glu1156Val
ENST00000675062.1:n.513A>T
ENST00000675078.1:c.3467A>T	ENSP00000501549.1:p.Glu1156Val
ENST00000675215.1:c.*2691A>T	ENSP00000502558.1:n.*2691A>T
ENST00000675233.1:n.5294A>T
ENST00000675321.1:c.3460+501A>T	ENSP00000502751.1:n.3460+501A>T
ENST00000675325.1:n.5424A>T
ENST00000675335.1:c.3498A>T	ENSP00000502182.1:n.3498A>T
ENST00000675400.1:n.5319A>T
ENST00000675406.1:c.3467A>T	ENSP00000501893.1:p.Glu1156Val
ENST00000675458.1:c.3560A>T	ENSP00000501754.1:n.3560A>T
ENST00000675507.1:n.5263A>T
ENST00000675535.1:c.*1094A>T	ENSP00000501667.1:n.*1094A>T
ENST00000675566.1:n.5325A>T
ENST00000675580.1:n.620A>T
ENST00000675602.1:n.6515A>T
ENST00000675647.1:n.4631A>T
ENST00000675711.1:c.3584A>T	ENSP00000502485.1:n.3584A>T
ENST00000675727.1:c.3467A>T	ENSP00000501722.1:p.Glu1156Val
ENST00000675748.1:n.5101A>T
ENST00000675765.1:c.*850A>T	ENSP00000502640.1:n.*850A>T
ENST00000675825.1:c.3509A>T	ENSP00000502632.1:p.Glu1170Val
ENST00000675877.1:n.5311A>T
ENST00000675893.1:c.*4536A>T	ENSP00000502001.1:n.*4536A>T
ENST00000675943.1:n.7082A>T
ENST00000675979.1:c.*2710A>T	ENSP00000502208.1:n.*2710A>T
ENST00000676044.1:c.*1127A>T	ENSP00000502378.1:n.*1127A>T
ENST00000676086.1:n.5252A>T
ENST00000676121.1:n.5295A>T
ENST00000676162.1:n.196A>T
ENST00000676237.1:c.3410A>T	ENSP00000501828.1:p.Glu1137Val
ENST00000676416.1:c.3167A>T	ENSP00000501660.1:p.Glu1056Val
ENST00000676424.1:n.5305A>T
ENST00000676429.1:n.7936A>T
ENST00000374647.9:c.3467A>T	ENSP00000363779.5:p.Glu1156Val
ENST00000467959.1:n.347A>T
ENST00000495759.5:c.607A>T
ENST00000537196.1:c.2420A>T	ENSP00000439367.1:p.Glu807Val
NM_003640.3:c.3467A>T , LRG_251t1:c.3467A>T	NP_003631.2:p.Glu1156Val
XM_005252285.2:c.3125A>T	XP_005252342.1:p.Glu1042Val
XM_011519136.1:c.3509A>T	XP_011517438.1:p.Glu1170Val
XM_011519137.1:c.3167A>T	XP_011517439.1:p.Glu1056Val
NM_001318360.1:c.3125A>T	NP_001305289.1:p.Glu1042Val
NM_001330749.1:c.2420A>T	NP_001317678.1:p.Glu807Val
NM_003640.4:c.3467A>T	NP_003631.2:p.Glu1156Val
XM_011519136.2:c.3509A>T	XP_011517438.1:p.Glu1170Val
XR_929859.3:n.3856A>T
NM_003640.5:c.3467A>T MANE Select	NP_003631.2:p.Glu1156Val
NM_001318360.2:c.3125A>T	NP_001305289.1:p.Glu1042Val
NM_001330749.2:c.2420A>T	NP_001317678.1:p.Glu807Val