Canonical Allele Identifier: CA340192433

Gene: RAD54L LRRC41

Linked Data

• dbSNP Id: rs121908690
• MyVariant Identifiers: chr1:g.46733212G>C (hg19) ; chr1:g.46267540G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46267540G>C , CM000663.2:g.46267540G>C	GRCh38
NC_000001.10:g.46733212G>C , CM000663.1:g.46733212G>C	GRCh37
NC_000001.9:g.46505799G>C	NCBI36
NG_012144.1:g.24846G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371975.9:c.973G>C (RAD54L) MANE Select	ENSP00000361043.4:p.Gly325Arg
ENST00000655446.1:c.*641G>C (RAD54L)	ENSP00000499451.1:n.*641G>C
ENST00000664182.1:n.36G>C (RAD54L)
ENST00000671528.1:c.973G>C (RAD54L)	ENSP00000499652.1:p.Gly325Arg
ENST00000371975.8:c.973G>C (RAD54L)	ENSP00000361043.4:p.Gly325Arg
ENST00000442598.5:c.973G>C (RAD54L)	ENSP00000396113.1:p.Gly325Arg
ENST00000472889.2:c.699G>C (RAD54L)
ENST00000473251.2:c.434G>C (RAD54L)
ENST00000476687.2:c.130G>C (RAD54L)	ENSP00000479734.1:p.Gly44Arg
ENST00000487700.1:n.428G>C (RAD54L)
ENST00000496156.5:c.638C>G (LRRC41)	ENSP00000477909.1:p.Pro213Arg
NM_001142548.1:c.973G>C (RAD54L)	NP_001136020.1:p.Gly325Arg
NM_003579.3:c.973G>C (RAD54L)	NP_003570.2:p.Gly325Arg
XM_006710975.2:c.433G>C (RAD54L)	XP_006711038.1:p.Gly145Arg
XM_011542299.1:c.199G>C (RAD54L)	XP_011540601.1:p.Gly67Arg
XM_011542300.1:c.199G>C (RAD54L)	XP_011540602.1:p.Gly67Arg
XM_006710975.3:c.433G>C (RAD54L)	XP_006711038.1:p.Gly145Arg
XM_011542299.2:c.199G>C (RAD54L)	XP_011540601.1:p.Gly67Arg
XM_011542300.3:c.199G>C (RAD54L)	XP_011540602.1:p.Gly67Arg
NM_003579.4:c.973G>C (RAD54L) MANE Select	NP_003570.2:p.Gly325Arg
NM_001370766.1:c.433G>C (RAD54L)	NP_001357695.1:p.Gly145Arg
NM_001142548.2:c.973G>C (RAD54L)	NP_001136020.1:p.Gly325Arg