Canonical Allele Identifier: CA1565194564

Gene: ELL2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.95920020A= , CM000667.2:g.95920020A=	GRCh38
NC_000005.9:g.95255724A= , CM000667.1:g.95255724A=	GRCh37
NC_000005.8:g.95281480A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237853.9:c.196-475T= MANE Select	ENSP00000237853.4:n.196-475T=
ENST00000237853.8:c.196-475T=	ENSP00000237853.4:n.196-475T=
ENST00000506628.1:n.262-13238T=
ENST00000508694.1:n.13-475T=
ENST00000513343.1:c.196-18940T=	ENSP00000423915.1:n.196-18940T=
ENST00000635633.1:c.231-475T=
NM_012081.5:c.196-475T=	NP_036213.2:n.196-475T=
XM_006714575.1:c.31-475T=	XP_006714638.1:n.31-475T=
XM_011543280.1:c.-79-6086T=	XP_011541582.1:n.-79-6086T=
XM_006714575.3:c.31-475T=	XP_006714638.1:n.31-475T=
XM_017009239.1:c.196-475T=	XP_016864728.1:n.196-475T=
XM_017009240.2:c.-201-475T=	XP_016864729.1:n.-201-475T=
XM_017009241.2:c.-79-6086T=	XP_016864730.1:n.-79-6086T=
XM_017009242.1:c.-201-475T=	XP_016864731.1:n.-201-475T=
XM_017009243.2:c.-454-475T=	XP_016864732.1:n.-454-475T=
NM_012081.6:c.196-475T= MANE Select	NP_036213.2:n.196-475T=