Canonical Allele Identifier: CA1871337588

Gene: ELP1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108899862G= , CM000671.2:g.108899862G=	GRCh38
NC_000009.11:g.111662142G= , CM000671.1:g.111662142G=	GRCh37
NC_000009.10:g.110701963G=	NCBI36
NG_008788.1:g.39467C= , LRG_251:g.39467C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374647.10:c.2164C= MANE Select	ENSP00000363779.5:p.Arg722=
ENST00000495759.6:c.*774C=	ENSP00000433514.2:n.*774C=
ENST00000674535.1:c.2164C=	ENSP00000502142.1:p.Arg722=
ENST00000674704.1:n.3971C=
ENST00000674836.1:n.2469C=
ENST00000674890.1:c.2164C=	ENSP00000501870.1:p.Arg722=
ENST00000674938.1:c.1822C=	ENSP00000502427.1:p.Arg608=
ENST00000674948.1:c.1822C=	ENSP00000501602.1:p.Arg608=
ENST00000675052.1:c.2164C=	ENSP00000502664.1:p.Arg722=
ENST00000675078.1:c.2164C=	ENSP00000501549.1:p.Arg722=
ENST00000675215.1:c.*1388C=	ENSP00000502558.1:n.*1388C=
ENST00000675233.1:n.3991C=
ENST00000675321.1:c.2164C=	ENSP00000502751.1:p.Arg722=
ENST00000675325.1:n.3960C=
ENST00000675335.1:c.2195C=	ENSP00000502182.1:n.2195C=
ENST00000675400.1:n.3837C=
ENST00000675406.1:c.2164C=	ENSP00000501893.1:p.Arg722=
ENST00000675458.1:c.2257C=	ENSP00000501754.1:n.2257C=
ENST00000675507.1:n.3960C=
ENST00000675535.1:c.2164C=	ENSP00000501667.1:p.Arg722=
ENST00000675566.1:n.3960C=
ENST00000675602.1:n.5212C=
ENST00000675647.1:n.2469C=
ENST00000675711.1:c.2164C=	ENSP00000502485.1:p.Arg722=
ENST00000675727.1:c.2164C=	ENSP00000501722.1:p.Arg722=
ENST00000675748.1:n.3798C=
ENST00000675765.1:c.2164C=	ENSP00000502640.1:p.Arg722=
ENST00000675825.1:c.2164C=	ENSP00000502632.1:p.Arg722=
ENST00000675877.1:n.2469C=
ENST00000675893.1:c.*3233C=	ENSP00000502001.1:n.*3233C=
ENST00000675943.1:n.5779C=
ENST00000675979.1:c.*1407C=	ENSP00000502208.1:n.*1407C=
ENST00000676044.1:c.2164C=	ENSP00000502378.1:p.Arg722=
ENST00000676086.1:n.3949C=
ENST00000676121.1:n.3992C=
ENST00000676237.1:c.2065C=	ENSP00000501828.1:p.Arg689=
ENST00000676416.1:c.1822C=	ENSP00000501660.1:p.Arg608=
ENST00000676424.1:n.3960C=
ENST00000676429.1:n.6633C=
ENST00000374647.9:c.2164C=	ENSP00000363779.5:p.Arg722=
ENST00000537196.1:c.1117C=	ENSP00000439367.1:p.Arg373=
NM_003640.3:c.2164C= , LRG_251t1:c.2164C=	NP_003631.2:p.Arg722=
XM_005252285.2:c.1822C=	XP_005252342.1:p.Arg608=
XM_011519136.1:c.2164C=	XP_011517438.1:p.Arg722=
XM_011519137.1:c.1822C=	XP_011517439.1:p.Arg608=
XR_929859.1:n.2480C=
NM_001318360.1:c.1822C=	NP_001305289.1:p.Arg608=
NM_001330749.1:c.1117C=	NP_001317678.1:p.Arg373=
NM_003640.4:c.2164C=	NP_003631.2:p.Arg722=
XM_011519136.2:c.2164C=	XP_011517438.1:p.Arg722=
XR_929859.3:n.2491C=
NM_003640.5:c.2164C= MANE Select	NP_003631.2:p.Arg722=
NM_001318360.2:c.1822C=	NP_001305289.1:p.Arg608=
NM_001330749.2:c.1117C=	NP_001317678.1:p.Arg373=