Canonical Allele Identifier: CA1565188652

Gene: ELL2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.95905459A= , CM000667.2:g.95905459A=	GRCh38
NC_000005.9:g.95241163A= , CM000667.1:g.95241163A=	GRCh37
NC_000005.8:g.95266919A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000237853.9:c.741+1064T= MANE Select	ENSP00000237853.4:n.741+1064T=
ENST00000237853.8:c.741+1064T=	ENSP00000237853.4:n.741+1064T=
ENST00000513343.1:c.196-4379T=	ENSP00000423915.1:n.196-4379T=
NM_012081.5:c.741+1064T=	NP_036213.2:n.741+1064T=
XM_006714575.1:c.576+1064T=	XP_006714638.1:n.576+1064T=
XM_011543280.1:c.345+1064T=	XP_011541582.1:n.345+1064T=
XM_006714575.3:c.576+1064T=	XP_006714638.1:n.576+1064T=
XM_017009239.1:c.741+1064T=	XP_016864728.1:n.741+1064T=
XM_017009240.2:c.345+1064T=	XP_016864729.1:n.345+1064T=
XM_017009241.2:c.345+1064T=	XP_016864730.1:n.345+1064T=
XM_017009242.1:c.345+1064T=	XP_016864731.1:n.345+1064T=
XM_017009243.2:c.186+1064T=	XP_016864732.1:n.186+1064T=
NM_012081.6:c.741+1064T= MANE Select	NP_036213.2:n.741+1064T=