Canonical Allele Identifier: CA2474107404

Gene: RAD54L

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46250498T= , CM000663.2:g.46250498T=	GRCh38
NC_000001.10:g.46716170T= , CM000663.1:g.46716170T=	GRCh37
NC_000001.9:g.46488757T=	NCBI36
NG_012144.1:g.7804T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371975.9:c.210+379T= MANE Select	ENSP00000361043.4:n.210+379T=
ENST00000469835.6:c.210+379T=	ENSP00000477172.2:n.210+379T=
ENST00000655446.1:c.210+379T=	ENSP00000499451.1:n.210+379T=
ENST00000657122.1:c.*112+379T=	ENSP00000499519.1:n.*112+379T=
ENST00000669994.1:c.210+379T=	ENSP00000499311.1:n.210+379T=
ENST00000671528.1:c.210+379T=	ENSP00000499652.1:n.210+379T=
ENST00000371975.8:c.210+379T=	ENSP00000361043.4:n.210+379T=
ENST00000442598.5:c.210+379T=	ENSP00000396113.1:n.210+379T=
ENST00000463715.5:c.-363+379T=	ENSP00000480207.1:n.-363+379T=
ENST00000469835.5:c.210+379T=	ENSP00000477172.1:n.210+379T=
ENST00000487700.1:n.207+379T=
ENST00000493032.5:c.-195+379T=	ENSP00000479995.1:n.-195+379T=
ENST00000493985.5:c.-331+379T=	ENSP00000479823.1:n.-331+379T=
NM_001142548.1:c.210+379T=	NP_001136020.1:n.210+379T=
NM_003579.3:c.210+379T=	NP_003570.2:n.210+379T=
XM_006710975.2:c.-331+379T=	XP_006711038.1:n.-331+379T=
XM_006710975.3:c.-331+379T=	XP_006711038.1:n.-331+379T=
NM_003579.4:c.210+379T= MANE Select	NP_003570.2:n.210+379T=
NM_001370766.1:c.-331+379T=	NP_001357695.1:n.-331+379T=
NM_001142548.2:c.210+379T=	NP_001136020.1:n.210+379T=