Canonical Allele Identifier: CA834475

Gene: RAD54L LRRC41

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46270754C>T , CM000663.2:g.46270754C>T	GRCh38
NC_000001.10:g.46736426C>T , CM000663.1:g.46736426C>T	GRCh37
NC_000001.9:g.46509013C>T	NCBI36
NG_012144.1:g.28060C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371975.9:c.1138C>T (RAD54L) MANE Select	ENSP00000361043.4:p.Arg380Trp
ENST00000655446.1:c.*806C>T (RAD54L)	ENSP00000499451.1:n.*806C>T
ENST00000661701.1:c.96C>T (RAD54L)
ENST00000664182.1:n.201C>T (RAD54L)
ENST00000671528.1:c.1138C>T (RAD54L)	ENSP00000499652.1:p.Arg380Trp
ENST00000371975.8:c.1138C>T (RAD54L)	ENSP00000361043.4:p.Arg380Trp
ENST00000442598.5:c.1138C>T (RAD54L)	ENSP00000396113.1:p.Arg380Trp
ENST00000473251.2:c.599C>T (RAD54L)
ENST00000476687.2:c.200-1712C>T (RAD54L)	ENSP00000479734.1:n.200-1712C>T
ENST00000496156.5:c.501-3077G>A (LRRC41)	ENSP00000477909.1:n.501-3077G>A
NM_001142548.1:c.1138C>T (RAD54L)	NP_001136020.1:p.Arg380Trp
NM_003579.3:c.1138C>T (RAD54L)	NP_003570.2:p.Arg380Trp
XM_006710975.2:c.598C>T (RAD54L)	XP_006711038.1:p.Arg200Trp
XM_011542299.1:c.364C>T (RAD54L)	XP_011540601.1:p.Arg122Trp
XM_011542300.1:c.364C>T (RAD54L)	XP_011540602.1:p.Arg122Trp
XM_006710975.3:c.598C>T (RAD54L)	XP_006711038.1:p.Arg200Trp
XM_011542299.2:c.364C>T (RAD54L)	XP_011540601.1:p.Arg122Trp
XM_011542300.3:c.364C>T (RAD54L)	XP_011540602.1:p.Arg122Trp
NM_003579.4:c.1138C>T (RAD54L) MANE Select	NP_003570.2:p.Arg380Trp
NM_001370766.1:c.598C>T (RAD54L)	NP_001357695.1:p.Arg200Trp
NM_001142548.2:c.1138C>T (RAD54L)	NP_001136020.1:p.Arg380Trp