Canonical Allele Identifier: CA2691095861

Gene: ELP1

Linked Data

• gnomAD v4: 9-108899972-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108899975_108899976del , CM000671.2:g.108899975_108899976del	GRCh38
NC_000009.11:g.111662255_111662256del , CM000671.1:g.111662255_111662256del	GRCh37
NC_000009.10:g.110702076_110702077del	NCBI36
NG_008788.1:g.39355_39356del , LRG_251:g.39355_39356del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374647.10:c.2131-79_2131-78del MANE Select	ENSP00000363779.5:n.2131-79_2131-78del
ENST00000495759.6:c.*741-79_*741-78del	ENSP00000433514.2:n.*741-79_*741-78del
ENST00000674535.1:c.2131-79_2131-78del	ENSP00000502142.1:n.2131-79_2131-78del
ENST00000674704.1:n.3938-79_3938-78del
ENST00000674836.1:n.2436-79_2436-78del
ENST00000674890.1:c.2131-79_2131-78del	ENSP00000501870.1:n.2131-79_2131-78del
ENST00000674938.1:c.1789-79_1789-78del	ENSP00000502427.1:n.1789-79_1789-78del
ENST00000674948.1:c.1789-79_1789-78del	ENSP00000501602.1:n.1789-79_1789-78del
ENST00000675052.1:c.2131-79_2131-78del	ENSP00000502664.1:n.2131-79_2131-78del
ENST00000675078.1:c.2131-79_2131-78del	ENSP00000501549.1:n.2131-79_2131-78del
ENST00000675215.1:c.*1355-79_*1355-78del	ENSP00000502558.1:n.*1355-79_*1355-78del
ENST00000675233.1:n.3958-79_3958-78del
ENST00000675321.1:c.2131-79_2131-78del	ENSP00000502751.1:n.2131-79_2131-78del
ENST00000675325.1:n.3927-79_3927-78del
ENST00000675335.1:c.2162-79_2162-78del	ENSP00000502182.1:n.2162-79_2162-78del
ENST00000675400.1:n.3804-79_3804-78del
ENST00000675406.1:c.2131-79_2131-78del	ENSP00000501893.1:n.2131-79_2131-78del
ENST00000675458.1:c.2224-79_2224-78del	ENSP00000501754.1:n.2224-79_2224-78del
ENST00000675507.1:n.3927-79_3927-78del
ENST00000675535.1:c.2131-79_2131-78del	ENSP00000501667.1:n.2131-79_2131-78del
ENST00000675566.1:n.3927-79_3927-78del
ENST00000675602.1:n.5179-79_5179-78del
ENST00000675647.1:n.2436-79_2436-78del
ENST00000675711.1:c.2131-79_2131-78del	ENSP00000502485.1:n.2131-79_2131-78del
ENST00000675727.1:c.2131-79_2131-78del	ENSP00000501722.1:n.2131-79_2131-78del
ENST00000675748.1:n.3765-79_3765-78del
ENST00000675765.1:c.2131-79_2131-78del	ENSP00000502640.1:n.2131-79_2131-78del
ENST00000675825.1:c.2131-79_2131-78del	ENSP00000502632.1:n.2131-79_2131-78del
ENST00000675877.1:n.2436-79_2436-78del
ENST00000675893.1:c.*3200-79_*3200-78del	ENSP00000502001.1:n.*3200-79_*3200-78del
ENST00000675943.1:n.5746-79_5746-78del
ENST00000675979.1:c.*1374-79_*1374-78del	ENSP00000502208.1:n.*1374-79_*1374-78del
ENST00000676044.1:c.2131-79_2131-78del	ENSP00000502378.1:n.2131-79_2131-78del
ENST00000676086.1:n.3916-79_3916-78del
ENST00000676121.1:n.3959-79_3959-78del
ENST00000676237.1:c.2032-79_2032-78del	ENSP00000501828.1:n.2032-79_2032-78del
ENST00000676416.1:c.1789-79_1789-78del	ENSP00000501660.1:n.1789-79_1789-78del
ENST00000676424.1:n.3927-79_3927-78del
ENST00000676429.1:n.6600-79_6600-78del
ENST00000374647.9:c.2131-79_2131-78del	ENSP00000363779.5:n.2131-79_2131-78del
ENST00000537196.1:c.1084-79_1084-78del	ENSP00000439367.1:n.1084-79_1084-78del
NM_003640.3:c.2131-79_2131-78del , LRG_251t1:c.2131-79_2131-78del	NP_003631.2:n.2131-79_2131-78del
XM_005252285.2:c.1789-79_1789-78del	XP_005252342.1:n.1789-79_1789-78del
XM_011519136.1:c.2131-79_2131-78del	XP_011517438.1:n.2131-79_2131-78del
XM_011519137.1:c.1789-79_1789-78del	XP_011517439.1:n.1789-79_1789-78del
XR_929859.1:n.2447-79_2447-78del
NM_001318360.1:c.1789-79_1789-78del	NP_001305289.1:n.1789-79_1789-78del
NM_001330749.1:c.1084-79_1084-78del	NP_001317678.1:n.1084-79_1084-78del
NM_003640.4:c.2131-79_2131-78del	NP_003631.2:n.2131-79_2131-78del
XM_011519136.2:c.2131-79_2131-78del	XP_011517438.1:n.2131-79_2131-78del
XR_929859.3:n.2458-79_2458-78del
NM_003640.5:c.2131-79_2131-78del MANE Select	NP_003631.2:n.2131-79_2131-78del
NM_001318360.2:c.1789-79_1789-78del	NP_001305289.1:n.1789-79_1789-78del
NM_001330749.2:c.1084-79_1084-78del	NP_001317678.1:n.1084-79_1084-78del