Canonical Allele Identifier: CA2474107265
Gene: RAD54L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46250152_46250154delinsCTG , CM000663.2:g.46250152_46250154delinsCTG GRCh38
NC_000001.10:g.46715824_46715826delinsCTG , CM000663.1:g.46715824_46715826delinsCTG GRCh37
NC_000001.9:g.46488411_46488413delinsCTG NCBI36
NG_012144.1:g.7458_7460delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000371975.9:c.210+33_210+35delinsCTG MANE Select ENSP00000361043.4:n.210+33_210+35delinsCTG
ENST00000469835.6:c.210+33_210+35delinsCTG ENSP00000477172.2:n.210+33_210+35delinsCTG
ENST00000655446.1:c.210+33_210+35delinsCTG ENSP00000499451.1:n.210+33_210+35delinsCTG
ENST00000657122.1:c.*112+33_*112+35delinsCTG ENSP00000499519.1:n.*112+33_*112+35delinsCTG
ENST00000669994.1:c.210+33_210+35delinsCTG ENSP00000499311.1:n.210+33_210+35delinsCTG
ENST00000671528.1:c.210+33_210+35delinsCTG ENSP00000499652.1:n.210+33_210+35delinsCTG
ENST00000371975.8:c.210+33_210+35delinsCTG ENSP00000361043.4:n.210+33_210+35delinsCTG
ENST00000442598.5:c.210+33_210+35delinsCTG ENSP00000396113.1:n.210+33_210+35delinsCTG
ENST00000463715.5:c.-363+33_-363+35delinsCTG ENSP00000480207.1:n.-363+33_-363+35delinsCTG
ENST00000469835.5:c.210+33_210+35delinsCTG ENSP00000477172.1:n.210+33_210+35delinsCTG
ENST00000487700.1:n.207+33_207+35delinsCTG
ENST00000493032.5:c.-195+33_-195+35delinsCTG ENSP00000479995.1:n.-195+33_-195+35delinsCTG
ENST00000493985.5:c.-331+33_-331+35delinsCTG ENSP00000479823.1:n.-331+33_-331+35delinsCTG
NM_001142548.1:c.210+33_210+35delinsCTG NP_001136020.1:n.210+33_210+35delinsCTG
NM_003579.3:c.210+33_210+35delinsCTG NP_003570.2:n.210+33_210+35delinsCTG
XM_006710975.2:c.-331+33_-331+35delinsCTG XP_006711038.1:n.-331+33_-331+35delinsCTG
XM_006710975.3:c.-331+33_-331+35delinsCTG XP_006711038.1:n.-331+33_-331+35delinsCTG
NM_003579.4:c.210+33_210+35delinsCTG MANE Select NP_003570.2:n.210+33_210+35delinsCTG
NM_001370766.1:c.-331+33_-331+35delinsCTG NP_001357695.1:n.-331+33_-331+35delinsCTG
NM_001142548.2:c.210+33_210+35delinsCTG NP_001136020.1:n.210+33_210+35delinsCTG