Canonical Allele Identifier: CA2558575279
Gene: REL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.60897668C>A , CM000664.2:g.60897668C>A GRCh38
NC_000002.11:g.61124803C>A , CM000664.1:g.61124803C>A GRCh37
NC_000002.10:g.60978307C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000699191.1:c.302+3123C>A ENSP00000514191.1:n.302+3123C>A
ENST00000699192.1:c.302+3123C>A ENSP00000514192.1:n.302+3123C>A
ENST00000699193.1:c.302+3123C>A ENSP00000514193.1:n.302+3123C>A
ENST00000699194.1:n.253+3123C>A
ENST00000394479.4:c.302+3123C>A MANE Select ENSP00000377989.4:n.302+3123C>A
ENST00000642725.1:c.150-1302C>A ENSP00000496299.1:n.150-1302C>A
ENST00000295025.12:c.302+3123C>A ENSP00000295025.7:n.302+3123C>A
ENST00000394479.3:c.302+3123C>A ENSP00000377989.3:n.302+3123C>A
NM_001291746.1:c.302+3123C>A NP_001278675.1:n.302+3123C>A
NM_002908.3:c.302+3123C>A NP_002899.1:n.302+3123C>A
XM_017004627.2:c.302+3123C>A XP_016860116.1:n.302+3123C>A
NM_001291746.2:c.302+3123C>A MANE Select NP_001278675.1:n.302+3123C>A
NM_002908.4:c.302+3123C>A NP_002899.1:n.302+3123C>A
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