Canonical Allele Identifier: CA1255111827

Gene: REL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.60908994G= , CM000664.2:g.60908994G=	GRCh38
NC_000002.11:g.61136129G= , CM000664.1:g.61136129G=	GRCh37
NC_000002.10:g.60989633G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001291746.2:c.395-7883G= MANE Select	NP_001278675.1:n.395-7883G=
ENST00000394479.4:c.395-7883G= MANE Select	ENSP00000377989.4:n.395-7883G=
NM_001291746.1:c.395-7883G=	NP_001278675.1:n.395-7883G=
NM_002908.3:c.395-7883G=	NP_002899.1:n.395-7883G=
NM_002908.4:c.395-7883G=	NP_002899.1:n.395-7883G=
ENST00000295025.12:c.395-7883G=	ENSP00000295025.7:n.395-7883G=
ENST00000394479.3:c.395-7883G=	ENSP00000377989.3:n.395-7883G=
ENST00000699191.1:c.395-7883G=	ENSP00000514191.1:n.395-7883G=
ENST00000699192.1:c.395-7883G=	ENSP00000514192.1:n.395-7883G=
ENST00000699193.1:c.303-7883G=	ENSP00000514193.1:n.303-7883G=
ENST00000699194.1:n.346-7883G=
XM_011533010.1:c.101-7883G=	XP_011531312.1:n.101-7883G=
XM_011533010.3:c.101-7883G=	XP_011531312.1:n.101-7883G=
XM_017004627.2:c.395-7883G=	XP_016860116.1:n.395-7883G=