Canonical Allele Identifier: CA834223

Gene: RAD54L

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46260058G>A , CM000663.2:g.46260058G>A	GRCh38
NC_000001.10:g.46725730G>A , CM000663.1:g.46725730G>A	GRCh37
NC_000001.9:g.46498317G>A	NCBI36
NG_012144.1:g.17364G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371975.9:c.366G>A MANE Select	ENSP00000361043.4:p.Glu122=
ENST00000469835.6:c.366G>A	ENSP00000477172.2:p.Glu122=
ENST00000655446.1:c.*34G>A	ENSP00000499451.1:n.*34G>A
ENST00000657122.1:c.*268G>A	ENSP00000499519.1:n.*268G>A
ENST00000668565.1:n.135G>A
ENST00000669994.1:c.366G>A	ENSP00000499311.1:p.Glu122=
ENST00000671528.1:c.366G>A	ENSP00000499652.1:p.Glu122=
ENST00000371975.8:c.366G>A	ENSP00000361043.4:p.Glu122=
ENST00000442598.5:c.366G>A	ENSP00000396113.1:p.Glu122=
ENST00000463715.5:c.-207G>A	ENSP00000480207.1:n.-207G>A
ENST00000469835.5:c.366G>A	ENSP00000477172.1:p.Glu122=
ENST00000472889.2:c.95G>A
ENST00000487700.1:n.363G>A
ENST00000493032.5:c.-133-484G>A	ENSP00000479995.1:n.-133-484G>A
ENST00000493985.5:c.-175G>A	ENSP00000479823.1:n.-175G>A
NM_001142548.1:c.366G>A	NP_001136020.1:p.Glu122=
NM_003579.3:c.366G>A	NP_003570.2:p.Glu122=
XM_006710975.2:c.-175G>A	XP_006711038.1:n.-175G>A
XM_011542299.1:c.-207G>A	XP_011540601.1:n.-207G>A
XM_011542300.1:c.-50G>A	XP_011540602.1:n.-50G>A
XM_006710975.3:c.-175G>A	XP_006711038.1:n.-175G>A
XM_011542299.2:c.-207G>A	XP_011540601.1:n.-207G>A
XM_011542300.3:c.-50G>A	XP_011540602.1:n.-50G>A
NM_003579.4:c.366G>A MANE Select	NP_003570.2:p.Glu122=
NM_001370766.1:c.-175G>A	NP_001357695.1:n.-175G>A
NM_001142548.2:c.366G>A	NP_001136020.1:p.Glu122=