Canonical Allele Identifier: CA834420
Gene: RAD54L HGNC NCBI
LRRC41 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46267461A>G , CM000663.2:g.46267461A>G GRCh38
NC_000001.10:g.46733133A>G , CM000663.1:g.46733133A>G GRCh37
NC_000001.9:g.46505720A>G NCBI36
NG_012144.1:g.24767A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371975.9:c.894A>G (RAD54L) MANE Select ENSP00000361043.4:p.Gly298=
ENST00000655446.1:c.*562A>G (RAD54L) ENSP00000499451.1:n.*562A>G
ENST00000671528.1:c.894A>G (RAD54L) ENSP00000499652.1:p.Gly298=
ENST00000371975.8:c.894A>G (RAD54L) ENSP00000361043.4:p.Gly298=
ENST00000442598.5:c.894A>G (RAD54L) ENSP00000396113.1:p.Gly298=
ENST00000472889.2:c.620A>G (RAD54L)
ENST00000473251.2:c.355A>G (RAD54L)
ENST00000476687.2:c.51A>G (RAD54L) ENSP00000479734.1:p.Gly17=
ENST00000487700.1:n.397-48A>G (RAD54L)
ENST00000496156.5:c.683+34T>C (LRRC41) ENSP00000477909.1:n.683+34T>C
NM_001142548.1:c.894A>G (RAD54L) NP_001136020.1:p.Gly298=
NM_003579.3:c.894A>G (RAD54L) NP_003570.2:p.Gly298=
XM_006710975.2:c.354A>G (RAD54L) XP_006711038.1:p.Gly118=
XM_011542299.1:c.120A>G (RAD54L) XP_011540601.1:p.Gly40=
XM_011542300.1:c.120A>G (RAD54L) XP_011540602.1:p.Gly40=
XM_006710975.3:c.354A>G (RAD54L) XP_006711038.1:p.Gly118=
XM_011542299.2:c.120A>G (RAD54L) XP_011540601.1:p.Gly40=
XM_011542300.3:c.120A>G (RAD54L) XP_011540602.1:p.Gly40=
NM_003579.4:c.894A>G (RAD54L) MANE Select NP_003570.2:p.Gly298=
NM_001370766.1:c.354A>G (RAD54L) NP_001357695.1:p.Gly118=
NM_001142548.2:c.894A>G (RAD54L) NP_001136020.1:p.Gly298=