Canonical Allele Identifier: CA374414920

Gene: ELP1

Linked Data

• MyVariant Identifiers: chr9:g.111651643T>G (hg19) ; chr9:g.108889363T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108889363T>G , CM000671.2:g.108889363T>G	GRCh38
NC_000009.11:g.111651643T>G , CM000671.1:g.111651643T>G	GRCh37
NC_000009.10:g.110691464T>G	NCBI36
NG_008788.1:g.49966A>C , LRG_251:g.49966A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374647.10:c.3191A>C MANE Select	ENSP00000363779.5:p.Asp1064Ala
ENST00000495759.6:c.*1801A>C	ENSP00000433514.2:n.*1801A>C
ENST00000674535.1:c.3191A>C	ENSP00000502142.1:p.Asp1064Ala
ENST00000674704.1:n.6276A>C
ENST00000674836.1:n.3804A>C
ENST00000674890.1:c.*426A>C	ENSP00000501870.1:n.*426A>C
ENST00000674938.1:c.2849A>C	ENSP00000502427.1:p.Asp950Ala
ENST00000674948.1:c.2849A>C	ENSP00000501602.1:p.Asp950Ala
ENST00000675052.1:c.3191A>C	ENSP00000502664.1:p.Asp1064Ala
ENST00000675078.1:c.3191A>C	ENSP00000501549.1:p.Asp1064Ala
ENST00000675215.1:c.*2415A>C	ENSP00000502558.1:n.*2415A>C
ENST00000675233.1:n.5018A>C
ENST00000675321.1:c.3191A>C	ENSP00000502751.1:p.Asp1064Ala
ENST00000675325.1:n.5148A>C
ENST00000675335.1:c.3222A>C	ENSP00000502182.1:n.3222A>C
ENST00000675400.1:n.4926A>C
ENST00000675406.1:c.3191A>C	ENSP00000501893.1:p.Asp1064Ala
ENST00000675458.1:c.3284A>C	ENSP00000501754.1:n.3284A>C
ENST00000675507.1:n.4987A>C
ENST00000675535.1:c.*818A>C	ENSP00000501667.1:n.*818A>C
ENST00000675566.1:n.5049A>C
ENST00000675602.1:n.6239A>C
ENST00000675647.1:n.4355A>C
ENST00000675711.1:c.3191A>C	ENSP00000502485.1:p.Asp1064Ala
ENST00000675727.1:c.3191A>C	ENSP00000501722.1:p.Asp1064Ala
ENST00000675748.1:n.4825A>C
ENST00000675765.1:c.*574A>C	ENSP00000502640.1:n.*574A>C
ENST00000675825.1:c.3191A>C	ENSP00000502632.1:p.Asp1064Ala
ENST00000675877.1:n.3496A>C
ENST00000675893.1:c.*4260A>C	ENSP00000502001.1:n.*4260A>C
ENST00000675943.1:n.6806A>C
ENST00000675979.1:c.*2434A>C	ENSP00000502208.1:n.*2434A>C
ENST00000676044.1:c.*851A>C	ENSP00000502378.1:n.*851A>C
ENST00000676086.1:n.4976A>C
ENST00000676121.1:n.5019A>C
ENST00000676237.1:c.3092A>C	ENSP00000501828.1:p.Asp1031Ala
ENST00000676416.1:c.2849A>C	ENSP00000501660.1:p.Asp950Ala
ENST00000676424.1:n.4987A>C
ENST00000676429.1:n.7660A>C
ENST00000374647.9:c.3191A>C	ENSP00000363779.5:p.Asp1064Ala
ENST00000467959.1:n.71A>C
ENST00000495759.5:c.331A>C
ENST00000537196.1:c.2144A>C	ENSP00000439367.1:p.Asp715Ala
NM_003640.3:c.3191A>C , LRG_251t1:c.3191A>C	NP_003631.2:p.Asp1064Ala
XM_005252285.2:c.2849A>C	XP_005252342.1:p.Asp950Ala
XM_011519136.1:c.3191A>C	XP_011517438.1:p.Asp1064Ala
XM_011519137.1:c.2849A>C	XP_011517439.1:p.Asp950Ala
NM_001318360.1:c.2849A>C	NP_001305289.1:p.Asp950Ala
NM_001330749.1:c.2144A>C	NP_001317678.1:p.Asp715Ala
NM_003640.4:c.3191A>C	NP_003631.2:p.Asp1064Ala
XM_011519136.2:c.3191A>C	XP_011517438.1:p.Asp1064Ala
XR_929859.3:n.3580A>C
NM_003640.5:c.3191A>C MANE Select	NP_003631.2:p.Asp1064Ala
NM_001318360.2:c.2849A>C	NP_001305289.1:p.Asp950Ala
NM_001330749.2:c.2144A>C	NP_001317678.1:p.Asp715Ala