Canonical Allele Identifier: CA834556
Gene: RAD54L HGNC NCBI
LRRC41 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46272677C>T , CM000663.2:g.46272677C>T GRCh38
NC_000001.10:g.46738349C>T , CM000663.1:g.46738349C>T GRCh37
NC_000001.9:g.46510936C>T NCBI36
NG_012144.1:g.29983C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371975.9:c.1250C>T (RAD54L) MANE Select ENSP00000361043.4:p.Thr417Ile
ENST00000655446.1:c.*918C>T (RAD54L) ENSP00000499451.1:n.*918C>T
ENST00000661701.1:c.283C>T (RAD54L)
ENST00000664182.1:n.313C>T (RAD54L)
ENST00000671528.1:c.1250C>T (RAD54L) ENSP00000499652.1:p.Thr417Ile
ENST00000371975.8:c.1250C>T (RAD54L) ENSP00000361043.4:p.Thr417Ile
ENST00000442598.5:c.1250C>T (RAD54L) ENSP00000396113.1:p.Thr417Ile
ENST00000459678.2:c.42C>T (RAD54L)
ENST00000473251.2:c.711C>T (RAD54L)
ENST00000476687.2:c.280C>T (RAD54L) ENSP00000479734.1:n.280C>T
ENST00000488942.5:c.81C>T (RAD54L)
ENST00000496156.5:c.501-5000G>A (LRRC41) ENSP00000477909.1:n.501-5000G>A
NM_001142548.1:c.1250C>T (RAD54L) NP_001136020.1:p.Thr417Ile
NM_003579.3:c.1250C>T (RAD54L) NP_003570.2:p.Thr417Ile
XM_006710975.2:c.710C>T (RAD54L) XP_006711038.1:p.Thr237Ile
XM_011542299.1:c.476C>T (RAD54L) XP_011540601.1:p.Thr159Ile
XM_011542300.1:c.476C>T (RAD54L) XP_011540602.1:p.Thr159Ile
XM_006710975.3:c.710C>T (RAD54L) XP_006711038.1:p.Thr237Ile
XM_011542299.2:c.476C>T (RAD54L) XP_011540601.1:p.Thr159Ile
XM_011542300.3:c.476C>T (RAD54L) XP_011540602.1:p.Thr159Ile
NM_003579.4:c.1250C>T (RAD54L) MANE Select NP_003570.2:p.Thr417Ile
NM_001370766.1:c.710C>T (RAD54L) NP_001357695.1:p.Thr237Ile
NM_001142548.2:c.1250C>T (RAD54L) NP_001136020.1:p.Thr417Ile