Canonical Allele Identifier: CA21897849

Gene: RAD54L LRRC41

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46273660C>T , CM000663.2:g.46273660C>T	GRCh38
NC_000001.10:g.46739332C>T , CM000663.1:g.46739332C>T	GRCh37
NC_000001.9:g.46511919C>T	NCBI36
NG_012144.1:g.30966C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371975.9:c.1523C>T (RAD54L) MANE Select	ENSP00000361043.4:p.Thr508Ile
ENST00000655446.1:c.*1191C>T (RAD54L)	ENSP00000499451.1:n.*1191C>T
ENST00000661701.1:c.556C>T (RAD54L)
ENST00000664182.1:n.744C>T (RAD54L)
ENST00000671528.1:c.1523C>T (RAD54L)	ENSP00000499652.1:p.Thr508Ile
ENST00000371975.8:c.1523C>T (RAD54L)	ENSP00000361043.4:p.Thr508Ile
ENST00000442598.5:c.1523C>T (RAD54L)	ENSP00000396113.1:p.Thr508Ile
ENST00000459678.2:c.278+195C>T (RAD54L)
ENST00000476687.2:c.553C>T (RAD54L)	ENSP00000479734.1:n.553C>T
ENST00000488942.5:c.243C>T (RAD54L)
ENST00000496156.5:c.500+5522G>A (LRRC41)	ENSP00000477909.1:n.500+5522G>A
NM_001142548.1:c.1523C>T (RAD54L)	NP_001136020.1:p.Thr508Ile
NM_003579.3:c.1523C>T (RAD54L)	NP_003570.2:p.Thr508Ile
XM_006710975.2:c.983C>T (RAD54L)	XP_006711038.1:p.Thr328Ile
XM_011542299.1:c.749C>T (RAD54L)	XP_011540601.1:p.Thr250Ile
XM_011542300.1:c.749C>T (RAD54L)	XP_011540602.1:p.Thr250Ile
XM_006710975.3:c.983C>T (RAD54L)	XP_006711038.1:p.Thr328Ile
XM_011542299.2:c.749C>T (RAD54L)	XP_011540601.1:p.Thr250Ile
XM_011542300.3:c.749C>T (RAD54L)	XP_011540602.1:p.Thr250Ile
NM_003579.4:c.1523C>T (RAD54L) MANE Select	NP_003570.2:p.Thr508Ile
NM_001370766.1:c.983C>T (RAD54L)	NP_001357695.1:p.Thr328Ile
NM_001142548.2:c.1523C>T (RAD54L)	NP_001136020.1:p.Thr508Ile