Canonical Allele Identifier: CA374423312

Gene: ELP1

Linked Data

• MyVariant Identifiers: chr9:g.111662543T>G (hg19) ; chr9:g.108900263T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108900263T>G , CM000671.2:g.108900263T>G	GRCh38
NC_000009.11:g.111662543T>G , CM000671.1:g.111662543T>G	GRCh37
NC_000009.10:g.110702364T>G	NCBI36
NG_008788.1:g.39066A>C , LRG_251:g.39066A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000374647.10:c.2127A>C MANE Select	ENSP00000363779.5:p.Leu709Phe
ENST00000495759.6:c.*737A>C	ENSP00000433514.2:n.*737A>C
ENST00000674535.1:c.2127A>C	ENSP00000502142.1:p.Leu709Phe
ENST00000674704.1:n.3934A>C
ENST00000674836.1:n.2432A>C
ENST00000674890.1:c.2127A>C	ENSP00000501870.1:p.Leu709Phe
ENST00000674938.1:c.1785A>C	ENSP00000502427.1:p.Leu595Phe
ENST00000674948.1:c.1785A>C	ENSP00000501602.1:p.Leu595Phe
ENST00000675052.1:c.2127A>C	ENSP00000502664.1:p.Leu709Phe
ENST00000675078.1:c.2127A>C	ENSP00000501549.1:p.Leu709Phe
ENST00000675215.1:c.*1351A>C	ENSP00000502558.1:n.*1351A>C
ENST00000675233.1:n.3954A>C
ENST00000675321.1:c.2127A>C	ENSP00000502751.1:p.Leu709Phe
ENST00000675325.1:n.3923A>C
ENST00000675335.1:c.2158A>C	ENSP00000502182.1:n.2158A>C
ENST00000675400.1:n.3800A>C
ENST00000675406.1:c.2127A>C	ENSP00000501893.1:p.Leu709Phe
ENST00000675458.1:c.2220A>C	ENSP00000501754.1:n.2220A>C
ENST00000675507.1:n.3923A>C
ENST00000675535.1:c.2127A>C	ENSP00000501667.1:p.Leu709Phe
ENST00000675566.1:n.3923A>C
ENST00000675602.1:n.5175A>C
ENST00000675647.1:n.2432A>C
ENST00000675711.1:c.2127A>C	ENSP00000502485.1:p.Leu709Phe
ENST00000675727.1:c.2127A>C	ENSP00000501722.1:p.Leu709Phe
ENST00000675748.1:n.3761A>C
ENST00000675765.1:c.2127A>C	ENSP00000502640.1:p.Leu709Phe
ENST00000675825.1:c.2127A>C	ENSP00000502632.1:p.Leu709Phe
ENST00000675877.1:n.2432A>C
ENST00000675893.1:c.*3196A>C	ENSP00000502001.1:n.*3196A>C
ENST00000675943.1:n.5742A>C
ENST00000675979.1:c.*1370A>C	ENSP00000502208.1:n.*1370A>C
ENST00000676044.1:c.2127A>C	ENSP00000502378.1:p.Leu709Phe
ENST00000676086.1:n.3912A>C
ENST00000676121.1:n.3955A>C
ENST00000676237.1:c.2028A>C	ENSP00000501828.1:p.Leu676Phe
ENST00000676416.1:c.1785A>C	ENSP00000501660.1:p.Leu595Phe
ENST00000676424.1:n.3923A>C
ENST00000676429.1:n.6596A>C
ENST00000374647.9:c.2127A>C	ENSP00000363779.5:p.Leu709Phe
ENST00000537196.1:c.1080A>C	ENSP00000439367.1:p.Leu360Phe
NM_003640.3:c.2127A>C , LRG_251t1:c.2127A>C	NP_003631.2:p.Leu709Phe
XM_005252285.2:c.1785A>C	XP_005252342.1:p.Leu595Phe
XM_011519136.1:c.2127A>C	XP_011517438.1:p.Leu709Phe
XM_011519137.1:c.1785A>C	XP_011517439.1:p.Leu595Phe
XR_929859.1:n.2443A>C
NM_001318360.1:c.1785A>C	NP_001305289.1:p.Leu595Phe
NM_001330749.1:c.1080A>C	NP_001317678.1:p.Leu360Phe
NM_003640.4:c.2127A>C	NP_003631.2:p.Leu709Phe
XM_011519136.2:c.2127A>C	XP_011517438.1:p.Leu709Phe
XR_929859.3:n.2454A>C
NM_003640.5:c.2127A>C MANE Select	NP_003631.2:p.Leu709Phe
NM_001318360.2:c.1785A>C	NP_001305289.1:p.Leu595Phe
NM_001330749.2:c.1080A>C	NP_001317678.1:p.Leu360Phe