Canonical Allele Identifier: CA381389341
Gene: RELA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65655736G>A , CM000673.2:g.65655736G>A GRCh38
NC_000011.9:g.65423207G>A , CM000673.1:g.65423207G>A GRCh37
NC_000011.8:g.65179783G>A NCBI36
NG_029971.1:g.12237C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000406246.8:c.985C>T MANE Select ENSP00000384273.3:p.Arg329Ter
ENST00000308639.13:c.976C>T ENSP00000311508.9:p.Arg326Ter
ENST00000406246.7:c.985C>T ENSP00000384273.3:p.Arg329Ter
ENST00000525693.5:c.985C>T ENSP00000432537.1:p.Arg329Ter
ENST00000526257.1:c.186C>T
ENST00000526283.6:c.*89C>T ENSP00000435290.1:n.*89C>T
ENST00000531484.5:n.1169C>T
ENST00000532999.5:c.1018C>T ENSP00000433526.1:p.Arg340Ter
ENST00000612991.4:c.985C>T ENSP00000483705.1:p.Arg329Ter
ENST00000615805.4:c.676-32C>T ENSP00000479572.1:n.676-32C>T
NM_001145138.1:c.976C>T NP_001138610.1:p.Arg326Ter
NM_001243984.1:c.985C>T NP_001230913.1:p.Arg329Ter
NM_001243985.1:c.985C>T NP_001230914.1:p.Arg329Ter
NM_021975.3:c.985C>T NP_068810.3:p.Arg329Ter
XM_011545206.1:c.772C>T XP_011543508.1:p.Arg258Ter
XM_011545207.1:c.667C>T XP_011543509.1:p.Arg223Ter
XM_011545206.2:c.772C>T XP_011543508.1:p.Arg258Ter
XM_011545207.2:c.667C>T XP_011543509.1:p.Arg223Ter
NM_021975.4:c.985C>T MANE Select NP_068810.3:p.Arg329Ter
NM_001145138.2:c.976C>T NP_001138610.1:p.Arg326Ter
NM_001243984.2:c.985C>T NP_001230913.1:p.Arg329Ter
NM_001243985.2:c.985C>T NP_001230914.1:p.Arg329Ter