Canonical Allele Identifier: CA374419194

Gene: ELP1

Linked Data

• gnomAD v4: 9-108894063-G-T
• MyVariant Identifiers: chr9:g.111656343G>T (hg19) ; chr9:g.108894063G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.108894063G>T , CM000671.2:g.108894063G>T	GRCh38
NC_000009.11:g.111656343G>T , CM000671.1:g.111656343G>T	GRCh37
NC_000009.10:g.110696164G>T	NCBI36
NG_008788.1:g.45266C>A , LRG_251:g.45266C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000374647.10:c.2740C>A MANE Select	ENSP00000363779.5:p.Pro914Thr
ENST00000495759.6:c.*1350C>A	ENSP00000433514.2:n.*1350C>A
ENST00000674535.1:c.2740C>A	ENSP00000502142.1:p.Pro914Thr
ENST00000674704.1:n.5825C>A
ENST00000674836.1:n.3353C>A
ENST00000674890.1:c.2762C>A	ENSP00000501870.1:p.Ser921Tyr
ENST00000674938.1:c.2398C>A	ENSP00000502427.1:p.Pro800Thr
ENST00000674948.1:c.2398C>A	ENSP00000501602.1:p.Pro800Thr
ENST00000675052.1:c.2740C>A	ENSP00000502664.1:p.Pro914Thr
ENST00000675078.1:c.2740C>A	ENSP00000501549.1:p.Pro914Thr
ENST00000675215.1:c.*1964C>A	ENSP00000502558.1:n.*1964C>A
ENST00000675233.1:n.4567C>A
ENST00000675321.1:c.2740C>A	ENSP00000502751.1:p.Pro914Thr
ENST00000675325.1:n.4697C>A
ENST00000675335.1:c.2771C>A	ENSP00000502182.1:n.2771C>A
ENST00000675400.1:n.4475C>A
ENST00000675406.1:c.2740C>A	ENSP00000501893.1:p.Pro914Thr
ENST00000675458.1:c.2833C>A	ENSP00000501754.1:n.2833C>A
ENST00000675507.1:n.4536C>A
ENST00000675535.1:c.*367C>A	ENSP00000501667.1:n.*367C>A
ENST00000675566.1:n.4598C>A
ENST00000675602.1:n.5788C>A
ENST00000675647.1:n.3045C>A
ENST00000675711.1:c.2740C>A	ENSP00000502485.1:p.Pro914Thr
ENST00000675727.1:c.2740C>A	ENSP00000501722.1:p.Pro914Thr
ENST00000675748.1:n.4374C>A
ENST00000675765.1:c.*123C>A	ENSP00000502640.1:n.*123C>A
ENST00000675825.1:c.2740C>A	ENSP00000502632.1:p.Pro914Thr
ENST00000675877.1:n.3045C>A
ENST00000675893.1:c.*3809C>A	ENSP00000502001.1:n.*3809C>A
ENST00000675943.1:n.6355C>A
ENST00000675979.1:c.*1983C>A	ENSP00000502208.1:n.*1983C>A
ENST00000676044.1:c.*400C>A	ENSP00000502378.1:n.*400C>A
ENST00000676086.1:n.4525C>A
ENST00000676121.1:n.4568C>A
ENST00000676237.1:c.2641C>A	ENSP00000501828.1:p.Pro881Thr
ENST00000676416.1:c.2398C>A	ENSP00000501660.1:p.Pro800Thr
ENST00000676424.1:n.4536C>A
ENST00000676429.1:n.7209C>A
ENST00000374647.9:c.2740C>A	ENSP00000363779.5:p.Pro914Thr
ENST00000537196.1:c.1693C>A	ENSP00000439367.1:p.Pro565Thr
NM_003640.3:c.2740C>A , LRG_251t1:c.2740C>A	NP_003631.2:p.Pro914Thr
XM_005252285.2:c.2398C>A	XP_005252342.1:p.Pro800Thr
XM_011519136.1:c.2740C>A	XP_011517438.1:p.Pro914Thr
XM_011519137.1:c.2398C>A	XP_011517439.1:p.Pro800Thr
XR_929859.1:n.3118C>A
NM_001318360.1:c.2398C>A	NP_001305289.1:p.Pro800Thr
NM_001330749.1:c.1693C>A	NP_001317678.1:p.Pro565Thr
NM_003640.4:c.2740C>A	NP_003631.2:p.Pro914Thr
XM_011519136.2:c.2740C>A	XP_011517438.1:p.Pro914Thr
XR_929859.3:n.3129C>A
NM_003640.5:c.2740C>A MANE Select	NP_003631.2:p.Pro914Thr
NM_001318360.2:c.2398C>A	NP_001305289.1:p.Pro800Thr
NM_001330749.2:c.1693C>A	NP_001317678.1:p.Pro565Thr