Canonical Allele Identifier: CA374386211

Gene: ELP1

Linked Data

• MyVariant Identifiers: chr9:g.111679865C>G (hg19) ; chr9:g.108917585C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108917585C>G , CM000671.2:g.108917585C>G	GRCh38
NC_000009.11:g.111679865C>G , CM000671.1:g.111679865C>G	GRCh37
NC_000009.10:g.110719686C>G	NCBI36
NG_008788.1:g.21744G>C , LRG_251:g.21744G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374647.10:c.826G>C MANE Select	ENSP00000363779.5:p.Gly276Arg
ENST00000495759.6:c.552+5257G>C	ENSP00000433514.2:n.552+5257G>C
ENST00000674535.1:c.826G>C	ENSP00000502142.1:p.Gly276Arg
ENST00000674704.1:n.2633G>C
ENST00000674836.1:n.1131G>C
ENST00000674890.1:c.826G>C	ENSP00000501870.1:p.Gly276Arg
ENST00000674938.1:c.484G>C	ENSP00000502427.1:p.Gly162Arg
ENST00000674948.1:c.484G>C	ENSP00000501602.1:p.Gly162Arg
ENST00000675052.1:c.826G>C	ENSP00000502664.1:p.Gly276Arg
ENST00000675078.1:c.826G>C	ENSP00000501549.1:p.Gly276Arg
ENST00000675215.1:c.*50G>C	ENSP00000502558.1:n.*50G>C
ENST00000675233.1:n.2622G>C
ENST00000675321.1:c.826G>C	ENSP00000502751.1:p.Gly276Arg
ENST00000675325.1:n.2622G>C
ENST00000675335.1:c.826G>C	ENSP00000502182.1:p.Gly276Arg
ENST00000675400.1:n.2499G>C
ENST00000675406.1:c.826G>C	ENSP00000501893.1:p.Gly276Arg
ENST00000675458.1:c.919G>C	ENSP00000501754.1:n.919G>C
ENST00000675507.1:n.2622G>C
ENST00000675535.1:c.826G>C	ENSP00000501667.1:p.Gly276Arg
ENST00000675566.1:n.2622G>C
ENST00000675602.1:n.2625G>C
ENST00000675647.1:n.1131G>C
ENST00000675711.1:c.826G>C	ENSP00000502485.1:p.Gly276Arg
ENST00000675727.1:c.826G>C	ENSP00000501722.1:p.Gly276Arg
ENST00000675748.1:n.2460G>C
ENST00000675765.1:c.826G>C	ENSP00000502640.1:p.Gly276Arg
ENST00000675825.1:c.826G>C	ENSP00000502632.1:p.Gly276Arg
ENST00000675877.1:n.1131G>C
ENST00000675893.1:c.*1895G>C	ENSP00000502001.1:n.*1895G>C
ENST00000675943.1:n.2622G>C
ENST00000675979.1:c.*69G>C	ENSP00000502208.1:n.*69G>C
ENST00000676044.1:c.826G>C	ENSP00000502378.1:p.Gly276Arg
ENST00000676086.1:n.2622G>C
ENST00000676121.1:n.2654G>C
ENST00000676237.1:c.727G>C	ENSP00000501828.1:p.Gly243Arg
ENST00000676416.1:c.484G>C	ENSP00000501660.1:p.Gly162Arg
ENST00000676424.1:n.2622G>C
ENST00000676429.1:n.5295G>C
ENST00000374647.9:c.826G>C	ENSP00000363779.5:p.Gly276Arg
ENST00000537196.1:c.-222G>C	ENSP00000439367.1:n.-222G>C
NM_003640.3:c.826G>C , LRG_251t1:c.826G>C	NP_003631.2:p.Gly276Arg
XM_005252285.2:c.484G>C	XP_005252342.1:p.Gly162Arg
XM_011519136.1:c.826G>C	XP_011517438.1:p.Gly276Arg
XM_011519137.1:c.484G>C	XP_011517439.1:p.Gly162Arg
XR_929859.1:n.1142G>C
NM_001318360.1:c.484G>C	NP_001305289.1:p.Gly162Arg
NM_001330749.1:c.-222G>C	NP_001317678.1:n.-222G>C
NM_003640.4:c.826G>C	NP_003631.2:p.Gly276Arg
XM_011519136.2:c.826G>C	XP_011517438.1:p.Gly276Arg
XR_929859.3:n.1153G>C
NM_003640.5:c.826G>C MANE Select	NP_003631.2:p.Gly276Arg
NM_001318360.2:c.484G>C	NP_001305289.1:p.Gly162Arg
NM_001330749.2:c.-222G>C	NP_001317678.1:n.-222G>C