Canonical Allele Identifier: CA1001305192
Gene: RAD54L HGNC NCBI

Linked Data

dbSNP Id: rs1659749552

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46249840_46249842del , CM000663.2:g.46249840_46249842del GRCh38
NC_000001.10:g.46715512_46715514del , CM000663.1:g.46715512_46715514del GRCh37
NC_000001.9:g.46488099_46488101del NCBI36
NG_012144.1:g.7146_7148del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371975.9:c.91-160_91-158del MANE Select ENSP00000361043.4:n.91-160_91-158del
ENST00000469835.6:c.91-160_91-158del ENSP00000477172.2:n.91-160_91-158del
ENST00000655446.1:c.91-160_91-158del ENSP00000499451.1:n.91-160_91-158del
ENST00000657122.1:c.116-160_116-158del ENSP00000499519.1:n.116-160_116-158del
ENST00000668390.1:n.487-160_487-158del
ENST00000669994.1:c.91-160_91-158del ENSP00000499311.1:n.91-160_91-158del
ENST00000671528.1:c.91-160_91-158del ENSP00000499652.1:n.91-160_91-158del
ENST00000371975.8:c.91-160_91-158del ENSP00000361043.4:n.91-160_91-158del
ENST00000442598.5:c.91-160_91-158del ENSP00000396113.1:n.91-160_91-158del
ENST00000463715.5:c.-482-160_-482-158del ENSP00000480207.1:n.-482-160_-482-158del
ENST00000469835.5:c.91-160_91-158del ENSP00000477172.1:n.91-160_91-158del
ENST00000487700.1:n.88-160_88-158del
ENST00000493032.5:c.-314-160_-314-158del ENSP00000479995.1:n.-314-160_-314-158del
ENST00000493985.5:c.-450-160_-450-158del ENSP00000479823.1:n.-450-160_-450-158del
NM_001142548.1:c.91-160_91-158del NP_001136020.1:n.91-160_91-158del
NM_003579.3:c.91-160_91-158del NP_003570.2:n.91-160_91-158del
XM_006710975.2:c.-450-160_-450-158del XP_006711038.1:n.-450-160_-450-158del
XM_006710975.3:c.-450-160_-450-158del XP_006711038.1:n.-450-160_-450-158del
NM_003579.4:c.91-160_91-158del MANE Select NP_003570.2:n.91-160_91-158del
NM_001370766.1:c.-450-160_-450-158del NP_001357695.1:n.-450-160_-450-158del
NM_001142548.2:c.91-160_91-158del NP_001136020.1:n.91-160_91-158del