Canonical Allele Identifier: CA858473540

Gene: ELP1

Linked Data

• dbSNP Id: rs1332620443
• MyVariant Identifiers: chr9:g.111662502del (hg19) ; chr9:g.108900222del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108900222del , CM000671.2:g.108900222del	GRCh38
NC_000009.11:g.111662502del , CM000671.1:g.111662502del	GRCh37
NC_000009.10:g.110702323del	NCBI36
NG_008788.1:g.39107del , LRG_251:g.39107del

Transcript Alleles

HGVS	Amino-acid change
ENST00000374647.10:c.2130+38del MANE Select	ENSP00000363779.5:n.2130+38del
ENST00000495759.6:c.*740+38del	ENSP00000433514.2:n.*740+38del
ENST00000674535.1:c.2130+38del	ENSP00000502142.1:n.2130+38del
ENST00000674704.1:n.3937+38del
ENST00000674836.1:n.2435+38del
ENST00000674890.1:c.2130+38del	ENSP00000501870.1:n.2130+38del
ENST00000674938.1:c.1788+38del	ENSP00000502427.1:n.1788+38del
ENST00000674948.1:c.1788+38del	ENSP00000501602.1:n.1788+38del
ENST00000675052.1:c.2130+38del	ENSP00000502664.1:n.2130+38del
ENST00000675078.1:c.2130+38del	ENSP00000501549.1:n.2130+38del
ENST00000675215.1:c.*1354+38del	ENSP00000502558.1:n.*1354+38del
ENST00000675233.1:n.3957+38del
ENST00000675321.1:c.2130+38del	ENSP00000502751.1:n.2130+38del
ENST00000675325.1:n.3926+38del
ENST00000675335.1:c.2161+38del	ENSP00000502182.1:n.2161+38del
ENST00000675400.1:n.3803+38del
ENST00000675406.1:c.2130+38del	ENSP00000501893.1:n.2130+38del
ENST00000675458.1:c.2223+38del	ENSP00000501754.1:n.2223+38del
ENST00000675507.1:n.3926+38del
ENST00000675535.1:c.2130+38del	ENSP00000501667.1:n.2130+38del
ENST00000675566.1:n.3926+38del
ENST00000675602.1:n.5178+38del
ENST00000675647.1:n.2435+38del
ENST00000675711.1:c.2130+38del	ENSP00000502485.1:n.2130+38del
ENST00000675727.1:c.2130+38del	ENSP00000501722.1:n.2130+38del
ENST00000675748.1:n.3764+38del
ENST00000675765.1:c.2130+38del	ENSP00000502640.1:n.2130+38del
ENST00000675825.1:c.2130+38del	ENSP00000502632.1:n.2130+38del
ENST00000675877.1:n.2435+38del
ENST00000675893.1:c.*3199+38del	ENSP00000502001.1:n.*3199+38del
ENST00000675943.1:n.5745+38del
ENST00000675979.1:c.*1373+38del	ENSP00000502208.1:n.*1373+38del
ENST00000676044.1:c.2130+38del	ENSP00000502378.1:n.2130+38del
ENST00000676086.1:n.3915+38del
ENST00000676121.1:n.3958+38del
ENST00000676237.1:c.2031+38del	ENSP00000501828.1:n.2031+38del
ENST00000676416.1:c.1788+38del	ENSP00000501660.1:n.1788+38del
ENST00000676424.1:n.3926+38del
ENST00000676429.1:n.6599+38del
ENST00000374647.9:c.2130+38del	ENSP00000363779.5:n.2130+38del
ENST00000537196.1:c.1083+38del	ENSP00000439367.1:n.1083+38del
NM_003640.3:c.2130+38del , LRG_251t1:c.2130+38del	NP_003631.2:n.2130+38del
XM_005252285.2:c.1788+38del	XP_005252342.1:n.1788+38del
XM_011519136.1:c.2130+38del	XP_011517438.1:n.2130+38del
XM_011519137.1:c.1788+38del	XP_011517439.1:n.1788+38del
XR_929859.1:n.2446+38del
NM_001318360.1:c.1788+38del	NP_001305289.1:n.1788+38del
NM_001330749.1:c.1083+38del	NP_001317678.1:n.1083+38del
NM_003640.4:c.2130+38del	NP_003631.2:n.2130+38del
XM_011519136.2:c.2130+38del	XP_011517438.1:n.2130+38del
XR_929859.3:n.2457+38del
NM_003640.5:c.2130+38del MANE Select	NP_003631.2:n.2130+38del
NM_001318360.2:c.1788+38del	NP_001305289.1:n.1788+38del
NM_001330749.2:c.1083+38del	NP_001317678.1:n.1083+38del