Canonical Allele Identifier: CA2326387165

Gene: ELL

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18508061A= , CM000681.2:g.18508061A=	GRCh38
NC_000019.9:g.18618871A= , CM000681.1:g.18618871A=	GRCh37
NC_000019.8:g.18479871A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000262809.9:c.135+13860T= MANE Select	ENSP00000262809.3:n.135+13860T=
ENST00000262809.8:c.135+13860T=	ENSP00000262809.3:n.135+13860T=
ENST00000594635.6:c.135+13860T=	ENSP00000475681.2:n.135+13860T=
ENST00000596915.1:n.147+13860T=
NM_006532.3:c.135+13860T=	NP_006523.1:n.135+13860T=
XM_011528330.1:c.135+13860T=	XP_011526632.1:n.135+13860T=
XR_936207.1:n.209+13860T=
XM_011528330.3:c.135+13860T=	XP_011526632.2:n.135+13860T=
XM_017027335.1:c.-385+13860T=	XP_016882824.1:n.-385+13860T=
XR_001753769.2:n.140+13860T=
XR_936207.3:n.140+13860T=
NM_006532.4:c.135+13860T= MANE Select	NP_006523.1:n.135+13860T=