Canonical Allele Identifier: CA374428559

Gene: ELP1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108911009C>A , CM000671.2:g.108911009C>A	GRCh38
NC_000009.11:g.111673289C>A , CM000671.1:g.111673289C>A	GRCh37
NC_000009.10:g.110713110C>A	NCBI36
NG_008788.1:g.28320G>T , LRG_251:g.28320G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003640.5:c.1360+1G>T MANE Select	NP_003631.2:n.1360+1G>T
ENST00000374647.10:c.1360+1G>T MANE Select	ENSP00000363779.5:n.1360+1G>T
NM_001318360.1:c.1018+1G>T	NP_001305289.1:n.1018+1G>T
NM_001318360.2:c.1018+1G>T	NP_001305289.1:n.1018+1G>T
NM_001330749.1:c.313+1G>T	NP_001317678.1:n.313+1G>T
NM_001330749.2:c.313+1G>T	NP_001317678.1:n.313+1G>T
NM_003640.3:c.1360+1G>T , LRG_251t1:c.1360+1G>T	NP_003631.2:n.1360+1G>T
NM_003640.4:c.1360+1G>T	NP_003631.2:n.1360+1G>T
ENST00000374647.9:c.1360+1G>T	ENSP00000363779.5:n.1360+1G>T
ENST00000495759.6:c.553-2605G>T	ENSP00000433514.2:n.553-2605G>T
ENST00000537196.1:c.313+1G>T	ENSP00000439367.1:n.313+1G>T
ENST00000674535.1:c.1360+1G>T	ENSP00000502142.1:n.1360+1G>T
ENST00000674704.1:n.3167+1G>T
ENST00000674836.1:n.1665+1G>T
ENST00000674890.1:c.1360+1G>T	ENSP00000501870.1:n.1360+1G>T
ENST00000674938.1:c.1018+1G>T	ENSP00000502427.1:n.1018+1G>T
ENST00000674948.1:c.1018+1G>T	ENSP00000501602.1:n.1018+1G>T
ENST00000675052.1:c.1360+1G>T	ENSP00000502664.1:n.1360+1G>T
ENST00000675078.1:c.1360+1G>T	ENSP00000501549.1:n.1360+1G>T
ENST00000675215.1:c.*584+1G>T	ENSP00000502558.1:n.*584+1G>T
ENST00000675233.1:n.3187+1G>T
ENST00000675321.1:c.1360+1G>T	ENSP00000502751.1:n.1360+1G>T
ENST00000675325.1:n.3156+1G>T
ENST00000675335.1:c.1391+1G>T	ENSP00000502182.1:n.1391+1G>T
ENST00000675400.1:n.3033+1G>T
ENST00000675406.1:c.1360+1G>T	ENSP00000501893.1:n.1360+1G>T
ENST00000675458.1:c.1453+1G>T	ENSP00000501754.1:n.1453+1G>T
ENST00000675507.1:n.3156+1G>T
ENST00000675535.1:c.1360+1G>T	ENSP00000501667.1:n.1360+1G>T
ENST00000675566.1:n.3156+1G>T
ENST00000675602.1:n.4408+1G>T
ENST00000675647.1:n.1665+1G>T
ENST00000675711.1:c.1360+1G>T	ENSP00000502485.1:n.1360+1G>T
ENST00000675727.1:c.1360+1G>T	ENSP00000501722.1:n.1360+1G>T
ENST00000675748.1:n.2994+1G>T
ENST00000675765.1:c.1360+1G>T	ENSP00000502640.1:n.1360+1G>T
ENST00000675825.1:c.1360+1G>T	ENSP00000502632.1:n.1360+1G>T
ENST00000675877.1:n.1665+1G>T
ENST00000675893.1:c.*2429+1G>T	ENSP00000502001.1:n.*2429+1G>T
ENST00000675943.1:n.3156+1G>T
ENST00000675979.1:c.*603+1G>T	ENSP00000502208.1:n.*603+1G>T
ENST00000676044.1:c.1360+1G>T	ENSP00000502378.1:n.1360+1G>T
ENST00000676086.1:n.3156+1G>T
ENST00000676121.1:n.3188+1G>T
ENST00000676237.1:c.1261+1G>T	ENSP00000501828.1:n.1261+1G>T
ENST00000676416.1:c.1018+1G>T	ENSP00000501660.1:n.1018+1G>T
ENST00000676424.1:n.3156+1G>T
ENST00000676429.1:n.5829+1G>T
XM_005252285.2:c.1018+1G>T	XP_005252342.1:n.1018+1G>T
XM_011519136.1:c.1360+1G>T	XP_011517438.1:n.1360+1G>T
XM_011519136.2:c.1360+1G>T	XP_011517438.1:n.1360+1G>T
XM_011519137.1:c.1018+1G>T	XP_011517439.1:n.1018+1G>T
XR_929859.1:n.1676+1G>T
XR_929859.3:n.1687+1G>T