Canonical Allele Identifier: CA1255106126
Gene: REL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.60897659T= , CM000664.2:g.60897659T= GRCh38
NC_000002.11:g.61124794T= , CM000664.1:g.61124794T= GRCh37
NC_000002.10:g.60978298T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000699191.1:c.302+3114T= ENSP00000514191.1:n.302+3114T=
ENST00000699192.1:c.302+3114T= ENSP00000514192.1:n.302+3114T=
ENST00000699193.1:c.302+3114T= ENSP00000514193.1:n.302+3114T=
ENST00000699194.1:n.253+3114T=
ENST00000394479.4:c.302+3114T= MANE Select ENSP00000377989.4:n.302+3114T=
ENST00000642725.1:c.150-1311T= ENSP00000496299.1:n.150-1311T=
ENST00000295025.12:c.302+3114T= ENSP00000295025.7:n.302+3114T=
ENST00000394479.3:c.302+3114T= ENSP00000377989.3:n.302+3114T=
NM_001291746.1:c.302+3114T= NP_001278675.1:n.302+3114T=
NM_002908.3:c.302+3114T= NP_002899.1:n.302+3114T=
XM_017004627.2:c.302+3114T= XP_016860116.1:n.302+3114T=
NM_001291746.2:c.302+3114T= MANE Select NP_001278675.1:n.302+3114T=
NM_002908.4:c.302+3114T= NP_002899.1:n.302+3114T=