Canonical Allele Identifier: CA374414957

Gene: ELP1

Linked Data

• MyVariant Identifiers: chr9:g.111651652T>A (hg19) ; chr9:g.108889372T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108889372T>A , CM000671.2:g.108889372T>A	GRCh38
NC_000009.11:g.111651652T>A , CM000671.1:g.111651652T>A	GRCh37
NC_000009.10:g.110691473T>A	NCBI36
NG_008788.1:g.49957A>T , LRG_251:g.49957A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374647.10:c.3182A>T MANE Select	ENSP00000363779.5:p.Lys1061Met
ENST00000495759.6:c.*1792A>T	ENSP00000433514.2:n.*1792A>T
ENST00000674535.1:c.3182A>T	ENSP00000502142.1:p.Lys1061Met
ENST00000674704.1:n.6267A>T
ENST00000674836.1:n.3795A>T
ENST00000674890.1:c.*417A>T	ENSP00000501870.1:n.*417A>T
ENST00000674938.1:c.2840A>T	ENSP00000502427.1:p.Lys947Met
ENST00000674948.1:c.2840A>T	ENSP00000501602.1:p.Lys947Met
ENST00000675052.1:c.3182A>T	ENSP00000502664.1:p.Lys1061Met
ENST00000675078.1:c.3182A>T	ENSP00000501549.1:p.Lys1061Met
ENST00000675215.1:c.*2406A>T	ENSP00000502558.1:n.*2406A>T
ENST00000675233.1:n.5009A>T
ENST00000675321.1:c.3182A>T	ENSP00000502751.1:p.Lys1061Met
ENST00000675325.1:n.5139A>T
ENST00000675335.1:c.3213A>T	ENSP00000502182.1:n.3213A>T
ENST00000675400.1:n.4917A>T
ENST00000675406.1:c.3182A>T	ENSP00000501893.1:p.Lys1061Met
ENST00000675458.1:c.3275A>T	ENSP00000501754.1:n.3275A>T
ENST00000675507.1:n.4978A>T
ENST00000675535.1:c.*809A>T	ENSP00000501667.1:n.*809A>T
ENST00000675566.1:n.5040A>T
ENST00000675602.1:n.6230A>T
ENST00000675647.1:n.4346A>T
ENST00000675711.1:c.3182A>T	ENSP00000502485.1:p.Lys1061Met
ENST00000675727.1:c.3182A>T	ENSP00000501722.1:p.Lys1061Met
ENST00000675748.1:n.4816A>T
ENST00000675765.1:c.*565A>T	ENSP00000502640.1:n.*565A>T
ENST00000675825.1:c.3182A>T	ENSP00000502632.1:p.Lys1061Met
ENST00000675877.1:n.3487A>T
ENST00000675893.1:c.*4251A>T	ENSP00000502001.1:n.*4251A>T
ENST00000675943.1:n.6797A>T
ENST00000675979.1:c.*2425A>T	ENSP00000502208.1:n.*2425A>T
ENST00000676044.1:c.*842A>T	ENSP00000502378.1:n.*842A>T
ENST00000676086.1:n.4967A>T
ENST00000676121.1:n.5010A>T
ENST00000676237.1:c.3083A>T	ENSP00000501828.1:p.Lys1028Met
ENST00000676416.1:c.2840A>T	ENSP00000501660.1:p.Lys947Met
ENST00000676424.1:n.4978A>T
ENST00000676429.1:n.7651A>T
ENST00000374647.9:c.3182A>T	ENSP00000363779.5:p.Lys1061Met
ENST00000467959.1:n.62A>T
ENST00000495759.5:c.322A>T
ENST00000537196.1:c.2135A>T	ENSP00000439367.1:p.Lys712Met
NM_003640.3:c.3182A>T , LRG_251t1:c.3182A>T	NP_003631.2:p.Lys1061Met
XM_005252285.2:c.2840A>T	XP_005252342.1:p.Lys947Met
XM_011519136.1:c.3182A>T	XP_011517438.1:p.Lys1061Met
XM_011519137.1:c.2840A>T	XP_011517439.1:p.Lys947Met
NM_001318360.1:c.2840A>T	NP_001305289.1:p.Lys947Met
NM_001330749.1:c.2135A>T	NP_001317678.1:p.Lys712Met
NM_003640.4:c.3182A>T	NP_003631.2:p.Lys1061Met
XM_011519136.2:c.3182A>T	XP_011517438.1:p.Lys1061Met
XR_929859.3:n.3571A>T
NM_003640.5:c.3182A>T MANE Select	NP_003631.2:p.Lys1061Met
NM_001318360.2:c.2840A>T	NP_001305289.1:p.Lys947Met
NM_001330749.2:c.2135A>T	NP_001317678.1:p.Lys712Met