Canonical Allele Identifier: CA2579411595

Gene: ELP1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108899980_108899987del , CM000671.2:g.108899980_108899987del	GRCh38
NC_000009.11:g.111662260_111662267del , CM000671.1:g.111662260_111662267del	GRCh37
NC_000009.10:g.110702081_110702088del	NCBI36
NG_008788.1:g.39342_39349del , LRG_251:g.39342_39349del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374647.10:c.2131-92_2131-85del MANE Select	ENSP00000363779.5:n.2131-92_2131-85del
ENST00000495759.6:c.*741-92_*741-85del	ENSP00000433514.2:n.*741-92_*741-85del
ENST00000674535.1:c.2131-92_2131-85del	ENSP00000502142.1:n.2131-92_2131-85del
ENST00000674704.1:n.3938-92_3938-85del
ENST00000674836.1:n.2436-92_2436-85del
ENST00000674890.1:c.2131-92_2131-85del	ENSP00000501870.1:n.2131-92_2131-85del
ENST00000674938.1:c.1789-92_1789-85del	ENSP00000502427.1:n.1789-92_1789-85del
ENST00000674948.1:c.1789-92_1789-85del	ENSP00000501602.1:n.1789-92_1789-85del
ENST00000675052.1:c.2131-92_2131-85del	ENSP00000502664.1:n.2131-92_2131-85del
ENST00000675078.1:c.2131-92_2131-85del	ENSP00000501549.1:n.2131-92_2131-85del
ENST00000675215.1:c.*1355-92_*1355-85del	ENSP00000502558.1:n.*1355-92_*1355-85del
ENST00000675233.1:n.3958-92_3958-85del
ENST00000675321.1:c.2131-92_2131-85del	ENSP00000502751.1:n.2131-92_2131-85del
ENST00000675325.1:n.3927-92_3927-85del
ENST00000675335.1:c.2162-92_2162-85del	ENSP00000502182.1:n.2162-92_2162-85del
ENST00000675400.1:n.3804-92_3804-85del
ENST00000675406.1:c.2131-92_2131-85del	ENSP00000501893.1:n.2131-92_2131-85del
ENST00000675458.1:c.2224-92_2224-85del	ENSP00000501754.1:n.2224-92_2224-85del
ENST00000675507.1:n.3927-92_3927-85del
ENST00000675535.1:c.2131-92_2131-85del	ENSP00000501667.1:n.2131-92_2131-85del
ENST00000675566.1:n.3927-92_3927-85del
ENST00000675602.1:n.5179-92_5179-85del
ENST00000675647.1:n.2436-92_2436-85del
ENST00000675711.1:c.2131-92_2131-85del	ENSP00000502485.1:n.2131-92_2131-85del
ENST00000675727.1:c.2131-92_2131-85del	ENSP00000501722.1:n.2131-92_2131-85del
ENST00000675748.1:n.3765-92_3765-85del
ENST00000675765.1:c.2131-92_2131-85del	ENSP00000502640.1:n.2131-92_2131-85del
ENST00000675825.1:c.2131-92_2131-85del	ENSP00000502632.1:n.2131-92_2131-85del
ENST00000675877.1:n.2436-92_2436-85del
ENST00000675893.1:c.*3200-92_*3200-85del	ENSP00000502001.1:n.*3200-92_*3200-85del
ENST00000675943.1:n.5746-92_5746-85del
ENST00000675979.1:c.*1374-92_*1374-85del	ENSP00000502208.1:n.*1374-92_*1374-85del
ENST00000676044.1:c.2131-92_2131-85del	ENSP00000502378.1:n.2131-92_2131-85del
ENST00000676086.1:n.3916-92_3916-85del
ENST00000676121.1:n.3959-92_3959-85del
ENST00000676237.1:c.2032-92_2032-85del	ENSP00000501828.1:n.2032-92_2032-85del
ENST00000676416.1:c.1789-92_1789-85del	ENSP00000501660.1:n.1789-92_1789-85del
ENST00000676424.1:n.3927-92_3927-85del
ENST00000676429.1:n.6600-92_6600-85del
ENST00000374647.9:c.2131-92_2131-85del	ENSP00000363779.5:n.2131-92_2131-85del
ENST00000537196.1:c.1084-92_1084-85del	ENSP00000439367.1:n.1084-92_1084-85del
NM_003640.3:c.2131-92_2131-85del , LRG_251t1:c.2131-92_2131-85del	NP_003631.2:n.2131-92_2131-85del
XM_005252285.2:c.1789-92_1789-85del	XP_005252342.1:n.1789-92_1789-85del
XM_011519136.1:c.2131-92_2131-85del	XP_011517438.1:n.2131-92_2131-85del
XM_011519137.1:c.1789-92_1789-85del	XP_011517439.1:n.1789-92_1789-85del
XR_929859.1:n.2447-92_2447-85del
NM_001318360.1:c.1789-92_1789-85del	NP_001305289.1:n.1789-92_1789-85del
NM_001330749.1:c.1084-92_1084-85del	NP_001317678.1:n.1084-92_1084-85del
NM_003640.4:c.2131-92_2131-85del	NP_003631.2:n.2131-92_2131-85del
XM_011519136.2:c.2131-92_2131-85del	XP_011517438.1:n.2131-92_2131-85del
XR_929859.3:n.2458-92_2458-85del
NM_003640.5:c.2131-92_2131-85del MANE Select	NP_003631.2:n.2131-92_2131-85del
NM_001318360.2:c.1789-92_1789-85del	NP_001305289.1:n.1789-92_1789-85del
NM_001330749.2:c.1084-92_1084-85del	NP_001317678.1:n.1084-92_1084-85del