Canonical Allele Identifier: CA834785

Gene: RAD54L LRRC41

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46277973C>T , CM000663.2:g.46277973C>T	GRCh38
NC_000001.10:g.46743645C>T , CM000663.1:g.46743645C>T	GRCh37
NC_000001.9:g.46516232C>T	NCBI36
NG_012144.1:g.35279C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371975.9:c.2026C>T (RAD54L) MANE Select	ENSP00000361043.4:p.His676Tyr
ENST00000617190.5:c.*892G>A (LRRC41) MANE Select	ENSP00000477792.1:n.*892G>A
ENST00000655446.1:c.*1694C>T (RAD54L)	ENSP00000499451.1:n.*1694C>T
ENST00000661701.1:c.1059C>T (RAD54L)
ENST00000671528.1:c.2026C>T (RAD54L)	ENSP00000499652.1:p.His676Tyr
ENST00000371975.8:c.2026C>T (RAD54L)	ENSP00000361043.4:p.His676Tyr
ENST00000442598.5:c.2026C>T (RAD54L)	ENSP00000396113.1:p.His676Tyr
ENST00000459678.2:c.694C>T (RAD54L)
ENST00000488942.5:c.746C>T (RAD54L)
ENST00000496156.5:c.500+1209G>A (LRRC41)	ENSP00000477909.1:n.500+1209G>A
ENST00000617190.4:c.*892G>A (LRRC41)	ENSP00000477792.1:n.*892G>A
NM_001142548.1:c.2026C>T (RAD54L)	NP_001136020.1:p.His676Tyr
NM_003579.3:c.2026C>T (RAD54L)	NP_003570.2:p.His676Tyr
XM_006710975.2:c.1486C>T (RAD54L)	XP_006711038.1:p.His496Tyr
XM_011542299.1:c.1252C>T (RAD54L)	XP_011540601.1:p.His418Tyr
XM_011542300.1:c.1252C>T (RAD54L)	XP_011540602.1:p.His418Tyr
XM_006710975.3:c.1486C>T (RAD54L)	XP_006711038.1:p.His496Tyr
XM_011542299.2:c.1252C>T (RAD54L)	XP_011540601.1:p.His418Tyr
XM_011542300.3:c.1252C>T (RAD54L)	XP_011540602.1:p.His418Tyr
NM_003579.4:c.2026C>T (RAD54L) MANE Select	NP_003570.2:p.His676Tyr
NM_001370766.1:c.1486C>T (RAD54L)	NP_001357695.1:p.His496Tyr
NM_001142548.2:c.2026C>T (RAD54L)	NP_001136020.1:p.His676Tyr
NM_006369.5:c.*892G>A (LRRC41) MANE Select	NP_006360.3:n.*892G>A