Canonical Allele Identifier: CA374411976

Gene: ELP1

Linked Data

• MyVariant Identifiers: chr9:g.111641826G>T (hg19) ; chr9:g.108879546G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108879546G>T , CM000671.2:g.108879546G>T	GRCh38
NC_000009.11:g.111641826G>T , CM000671.1:g.111641826G>T	GRCh37
NC_000009.10:g.110681647G>T	NCBI36
NG_008788.1:g.59783C>A , LRG_251:g.59783C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000374647.10:c.3472C>A MANE Select	ENSP00000363779.5:p.Pro1158Thr
ENST00000495759.6:c.*2082C>A	ENSP00000433514.2:n.*2082C>A
ENST00000674535.1:c.3472C>A	ENSP00000502142.1:p.Pro1158Thr
ENST00000674704.1:n.6557C>A
ENST00000674740.1:n.355C>A
ENST00000674836.1:n.4085C>A
ENST00000674890.1:c.*707C>A	ENSP00000501870.1:n.*707C>A
ENST00000674938.1:c.3130C>A	ENSP00000502427.1:p.Pro1044Thr
ENST00000674948.1:c.3130C>A	ENSP00000501602.1:p.Pro1044Thr
ENST00000675052.1:c.3472C>A	ENSP00000502664.1:p.Pro1158Thr
ENST00000675062.1:n.518C>A
ENST00000675078.1:c.3472C>A	ENSP00000501549.1:p.Pro1158Thr
ENST00000675215.1:c.*2696C>A	ENSP00000502558.1:n.*2696C>A
ENST00000675233.1:n.5299C>A
ENST00000675321.1:c.3460+506C>A	ENSP00000502751.1:n.3460+506C>A
ENST00000675325.1:n.5429C>A
ENST00000675335.1:c.3503C>A	ENSP00000502182.1:n.3503C>A
ENST00000675400.1:n.5324C>A
ENST00000675406.1:c.3472C>A	ENSP00000501893.1:p.Pro1158Thr
ENST00000675458.1:c.3565C>A	ENSP00000501754.1:n.3565C>A
ENST00000675507.1:n.5268C>A
ENST00000675535.1:c.*1099C>A	ENSP00000501667.1:n.*1099C>A
ENST00000675566.1:n.5330C>A
ENST00000675580.1:n.625C>A
ENST00000675602.1:n.6520C>A
ENST00000675647.1:n.4636C>A
ENST00000675711.1:c.3589C>A	ENSP00000502485.1:n.3589C>A
ENST00000675727.1:c.3472C>A	ENSP00000501722.1:p.Pro1158Thr
ENST00000675748.1:n.5106C>A
ENST00000675765.1:c.*855C>A	ENSP00000502640.1:n.*855C>A
ENST00000675825.1:c.3514C>A	ENSP00000502632.1:p.Pro1172Thr
ENST00000675877.1:n.5316C>A
ENST00000675893.1:c.*4541C>A	ENSP00000502001.1:n.*4541C>A
ENST00000675943.1:n.7087C>A
ENST00000675979.1:c.*2715C>A	ENSP00000502208.1:n.*2715C>A
ENST00000676044.1:c.*1132C>A	ENSP00000502378.1:n.*1132C>A
ENST00000676086.1:n.5257C>A
ENST00000676121.1:n.5300C>A
ENST00000676162.1:n.201C>A
ENST00000676237.1:c.3415C>A	ENSP00000501828.1:p.Pro1139Thr
ENST00000676416.1:c.3172C>A	ENSP00000501660.1:p.Pro1058Thr
ENST00000676424.1:n.5310C>A
ENST00000676429.1:n.7941C>A
ENST00000374647.9:c.3472C>A	ENSP00000363779.5:p.Pro1158Thr
ENST00000467959.1:n.352C>A
ENST00000495759.5:c.612C>A
ENST00000537196.1:c.2425C>A	ENSP00000439367.1:p.Pro809Thr
NM_003640.3:c.3472C>A , LRG_251t1:c.3472C>A	NP_003631.2:p.Pro1158Thr
XM_005252285.2:c.3130C>A	XP_005252342.1:p.Pro1044Thr
XM_011519136.1:c.3514C>A	XP_011517438.1:p.Pro1172Thr
XM_011519137.1:c.3172C>A	XP_011517439.1:p.Pro1058Thr
NM_001318360.1:c.3130C>A	NP_001305289.1:p.Pro1044Thr
NM_001330749.1:c.2425C>A	NP_001317678.1:p.Pro809Thr
NM_003640.4:c.3472C>A	NP_003631.2:p.Pro1158Thr
XM_011519136.2:c.3514C>A	XP_011517438.1:p.Pro1172Thr
XR_929859.3:n.3861C>A
NM_003640.5:c.3472C>A MANE Select	NP_003631.2:p.Pro1158Thr
NM_001318360.2:c.3130C>A	NP_001305289.1:p.Pro1044Thr
NM_001330749.2:c.2425C>A	NP_001317678.1:p.Pro809Thr