Canonical Allele Identifier: CA197531447

Gene: ELP1

Linked Data

• dbSNP Id: rs992252304
• MyVariant Identifiers: chr9:g.111656268A>G (hg19) ; chr9:g.108893988A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108893988A>G , CM000671.2:g.108893988A>G	GRCh38
NC_000009.11:g.111656268A>G , CM000671.1:g.111656268A>G	GRCh37
NC_000009.10:g.110696089A>G	NCBI36
NG_008788.1:g.45341T>C , LRG_251:g.45341T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000374647.10:c.2815T>C MANE Select	ENSP00000363779.5:p.Tyr939His
ENST00000495759.6:c.*1425T>C	ENSP00000433514.2:n.*1425T>C
ENST00000674535.1:c.2815T>C	ENSP00000502142.1:p.Tyr939His
ENST00000674704.1:n.5900T>C
ENST00000674836.1:n.3428T>C
ENST00000674890.1:c.*50T>C	ENSP00000501870.1:n.*50T>C
ENST00000674938.1:c.2473T>C	ENSP00000502427.1:p.Tyr825His
ENST00000674948.1:c.2473T>C	ENSP00000501602.1:p.Tyr825His
ENST00000675052.1:c.2815T>C	ENSP00000502664.1:p.Tyr939His
ENST00000675078.1:c.2815T>C	ENSP00000501549.1:p.Tyr939His
ENST00000675215.1:c.*2039T>C	ENSP00000502558.1:n.*2039T>C
ENST00000675233.1:n.4642T>C
ENST00000675321.1:c.2815T>C	ENSP00000502751.1:p.Tyr939His
ENST00000675325.1:n.4772T>C
ENST00000675335.1:c.2846T>C	ENSP00000502182.1:n.2846T>C
ENST00000675400.1:n.4550T>C
ENST00000675406.1:c.2815T>C	ENSP00000501893.1:p.Tyr939His
ENST00000675458.1:c.2908T>C	ENSP00000501754.1:n.2908T>C
ENST00000675507.1:n.4611T>C
ENST00000675535.1:c.*442T>C	ENSP00000501667.1:n.*442T>C
ENST00000675566.1:n.4673T>C
ENST00000675602.1:n.5863T>C
ENST00000675647.1:n.3120T>C
ENST00000675711.1:c.2815T>C	ENSP00000502485.1:p.Tyr939His
ENST00000675727.1:c.2815T>C	ENSP00000501722.1:p.Tyr939His
ENST00000675748.1:n.4449T>C
ENST00000675765.1:c.*198T>C	ENSP00000502640.1:n.*198T>C
ENST00000675825.1:c.2815T>C	ENSP00000502632.1:p.Tyr939His
ENST00000675877.1:n.3120T>C
ENST00000675893.1:c.*3884T>C	ENSP00000502001.1:n.*3884T>C
ENST00000675943.1:n.6430T>C
ENST00000675979.1:c.*2058T>C	ENSP00000502208.1:n.*2058T>C
ENST00000676044.1:c.*475T>C	ENSP00000502378.1:n.*475T>C
ENST00000676086.1:n.4600T>C
ENST00000676121.1:n.4643T>C
ENST00000676237.1:c.2716T>C	ENSP00000501828.1:p.Tyr906His
ENST00000676416.1:c.2473T>C	ENSP00000501660.1:p.Tyr825His
ENST00000676424.1:n.4611T>C
ENST00000676429.1:n.7284T>C
ENST00000374647.9:c.2815T>C	ENSP00000363779.5:p.Tyr939His
ENST00000537196.1:c.1768T>C	ENSP00000439367.1:p.Tyr590His
NM_003640.3:c.2815T>C , LRG_251t1:c.2815T>C	NP_003631.2:p.Tyr939His
XM_005252285.2:c.2473T>C	XP_005252342.1:p.Tyr825His
XM_011519136.1:c.2815T>C	XP_011517438.1:p.Tyr939His
XM_011519137.1:c.2473T>C	XP_011517439.1:p.Tyr825His
XR_929859.1:n.3193T>C
NM_001318360.1:c.2473T>C	NP_001305289.1:p.Tyr825His
NM_001330749.1:c.1768T>C	NP_001317678.1:p.Tyr590His
NM_003640.4:c.2815T>C	NP_003631.2:p.Tyr939His
XM_011519136.2:c.2815T>C	XP_011517438.1:p.Tyr939His
XR_929859.3:n.3204T>C
NM_003640.5:c.2815T>C MANE Select	NP_003631.2:p.Tyr939His
NM_001318360.2:c.2473T>C	NP_001305289.1:p.Tyr825His
NM_001330749.2:c.1768T>C	NP_001317678.1:p.Tyr590His