Canonical Allele Identifier: CA834675
Gene: RAD54L HGNC NCBI
LRRC41 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46274142T>C , CM000663.2:g.46274142T>C GRCh38
NC_000001.10:g.46739814T>C , CM000663.1:g.46739814T>C GRCh37
NC_000001.9:g.46512401T>C NCBI36
NG_012144.1:g.31448T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371975.9:c.1615T>C (RAD54L) MANE Select ENSP00000361043.4:p.Leu539=
ENST00000655446.1:c.*1283T>C (RAD54L) ENSP00000499451.1:n.*1283T>C
ENST00000661701.1:c.648T>C (RAD54L)
ENST00000671528.1:c.1615T>C (RAD54L) ENSP00000499652.1:p.Leu539=
ENST00000371975.8:c.1615T>C (RAD54L) ENSP00000361043.4:p.Leu539=
ENST00000442598.5:c.1615T>C (RAD54L) ENSP00000396113.1:p.Leu539=
ENST00000459678.2:c.283T>C (RAD54L)
ENST00000488942.5:c.335T>C (RAD54L)
ENST00000496156.5:c.500+5040A>G (LRRC41) ENSP00000477909.1:n.500+5040A>G
NM_001142548.1:c.1615T>C (RAD54L) NP_001136020.1:p.Leu539=
NM_003579.3:c.1615T>C (RAD54L) NP_003570.2:p.Leu539=
XM_006710975.2:c.1075T>C (RAD54L) XP_006711038.1:p.Leu359=
XM_011542299.1:c.841T>C (RAD54L) XP_011540601.1:p.Leu281=
XM_011542300.1:c.841T>C (RAD54L) XP_011540602.1:p.Leu281=
XM_006710975.3:c.1075T>C (RAD54L) XP_006711038.1:p.Leu359=
XM_011542299.2:c.841T>C (RAD54L) XP_011540601.1:p.Leu281=
XM_011542300.3:c.841T>C (RAD54L) XP_011540602.1:p.Leu281=
NM_003579.4:c.1615T>C (RAD54L) MANE Select NP_003570.2:p.Leu539=
NM_001370766.1:c.1075T>C (RAD54L) NP_001357695.1:p.Leu359=
NM_001142548.2:c.1615T>C (RAD54L) NP_001136020.1:p.Leu539=