Canonical Allele Identifier: CA2581774613

Gene: REL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.60897715T>G , CM000664.2:g.60897715T>G	GRCh38
NC_000002.11:g.61124850T>G , CM000664.1:g.61124850T>G	GRCh37
NC_000002.10:g.60978354T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000699191.1:c.302+3170T>G	ENSP00000514191.1:n.302+3170T>G
ENST00000699192.1:c.302+3170T>G	ENSP00000514192.1:n.302+3170T>G
ENST00000699193.1:c.302+3170T>G	ENSP00000514193.1:n.302+3170T>G
ENST00000699194.1:n.253+3170T>G
ENST00000394479.4:c.302+3170T>G MANE Select	ENSP00000377989.4:n.302+3170T>G
ENST00000642725.1:c.150-1255T>G	ENSP00000496299.1:n.150-1255T>G
ENST00000295025.12:c.302+3170T>G	ENSP00000295025.7:n.302+3170T>G
ENST00000394479.3:c.302+3170T>G	ENSP00000377989.3:n.302+3170T>G
NM_001291746.1:c.302+3170T>G	NP_001278675.1:n.302+3170T>G
NM_002908.3:c.302+3170T>G	NP_002899.1:n.302+3170T>G
XM_017004627.2:c.302+3170T>G	XP_016860116.1:n.302+3170T>G
NM_001291746.2:c.302+3170T>G MANE Select	NP_001278675.1:n.302+3170T>G
NM_002908.4:c.302+3170T>G	NP_002899.1:n.302+3170T>G