Canonical Allele Identifier: CA5174792

Gene: ELP1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108900364C>T , CM000671.2:g.108900364C>T	GRCh38
NC_000009.11:g.111662644C>T , CM000671.1:g.111662644C>T	GRCh37
NC_000009.10:g.110702465C>T	NCBI36
NG_008788.1:g.38965G>A , LRG_251:g.38965G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003640.5:c.2026G>A MANE Select	NP_003631.2:p.Gly676Ser
ENST00000374647.10:c.2026G>A MANE Select	ENSP00000363779.5:p.Gly676Ser
NM_001318360.1:c.1684G>A	NP_001305289.1:p.Gly562Ser
NM_001318360.2:c.1684G>A	NP_001305289.1:p.Gly562Ser
NM_001330749.1:c.979G>A	NP_001317678.1:p.Gly327Ser
NM_001330749.2:c.979G>A	NP_001317678.1:p.Gly327Ser
NM_003640.3:c.2026G>A , LRG_251t1:c.2026G>A	NP_003631.2:p.Gly676Ser
NM_003640.4:c.2026G>A	NP_003631.2:p.Gly676Ser
ENST00000374647.9:c.2026G>A	ENSP00000363779.5:p.Gly676Ser
ENST00000495759.6:c.*636G>A	ENSP00000433514.2:n.*636G>A
ENST00000537196.1:c.979G>A	ENSP00000439367.1:p.Gly327Ser
ENST00000674535.1:c.2026G>A	ENSP00000502142.1:p.Gly676Ser
ENST00000674704.1:n.3833G>A
ENST00000674836.1:n.2331G>A
ENST00000674890.1:c.2026G>A	ENSP00000501870.1:p.Gly676Ser
ENST00000674938.1:c.1684G>A	ENSP00000502427.1:p.Gly562Ser
ENST00000674948.1:c.1684G>A	ENSP00000501602.1:p.Gly562Ser
ENST00000675052.1:c.2026G>A	ENSP00000502664.1:p.Gly676Ser
ENST00000675078.1:c.2026G>A	ENSP00000501549.1:p.Gly676Ser
ENST00000675215.1:c.*1250G>A	ENSP00000502558.1:n.*1250G>A
ENST00000675233.1:n.3853G>A
ENST00000675321.1:c.2026G>A	ENSP00000502751.1:p.Gly676Ser
ENST00000675325.1:n.3822G>A
ENST00000675335.1:c.2057G>A	ENSP00000502182.1:n.2057G>A
ENST00000675400.1:n.3699G>A
ENST00000675406.1:c.2026G>A	ENSP00000501893.1:p.Gly676Ser
ENST00000675458.1:c.2119G>A	ENSP00000501754.1:n.2119G>A
ENST00000675507.1:n.3822G>A
ENST00000675535.1:c.2026G>A	ENSP00000501667.1:p.Gly676Ser
ENST00000675566.1:n.3822G>A
ENST00000675602.1:n.5074G>A
ENST00000675647.1:n.2331G>A
ENST00000675711.1:c.2026G>A	ENSP00000502485.1:p.Gly676Ser
ENST00000675727.1:c.2026G>A	ENSP00000501722.1:p.Gly676Ser
ENST00000675748.1:n.3660G>A
ENST00000675765.1:c.2026G>A	ENSP00000502640.1:p.Gly676Ser
ENST00000675825.1:c.2026G>A	ENSP00000502632.1:p.Gly676Ser
ENST00000675877.1:n.2331G>A
ENST00000675893.1:c.*3095G>A	ENSP00000502001.1:n.*3095G>A
ENST00000675943.1:n.5641G>A
ENST00000675979.1:c.*1269G>A	ENSP00000502208.1:n.*1269G>A
ENST00000676044.1:c.2026G>A	ENSP00000502378.1:p.Gly676Ser
ENST00000676086.1:n.3811G>A
ENST00000676121.1:n.3854G>A
ENST00000676237.1:c.1927G>A	ENSP00000501828.1:p.Gly643Ser
ENST00000676416.1:c.1684G>A	ENSP00000501660.1:p.Gly562Ser
ENST00000676424.1:n.3822G>A
ENST00000676429.1:n.6495G>A
XM_005252285.2:c.1684G>A	XP_005252342.1:p.Gly562Ser
XM_011519136.1:c.2026G>A	XP_011517438.1:p.Gly676Ser
XM_011519136.2:c.2026G>A	XP_011517438.1:p.Gly676Ser
XM_011519137.1:c.1684G>A	XP_011517439.1:p.Gly562Ser
XR_929859.1:n.2342G>A
XR_929859.3:n.2353G>A