Canonical Allele Identifier: CA21901531
Gene: RAD54L HGNC NCBI

Linked Data

dbSNP Id: rs1010537153

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46249884_46249885del , CM000663.2:g.46249884_46249885del GRCh38
NC_000001.10:g.46715556_46715557del , CM000663.1:g.46715556_46715557del GRCh37
NC_000001.9:g.46488143_46488144del NCBI36
NG_012144.1:g.7190_7191del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371975.9:c.91-116_91-115del MANE Select ENSP00000361043.4:n.91-116_91-115del
ENST00000469835.6:c.91-116_91-115del ENSP00000477172.2:n.91-116_91-115del
ENST00000655446.1:c.91-116_91-115del ENSP00000499451.1:n.91-116_91-115del
ENST00000657122.1:c.116-116_116-115del ENSP00000499519.1:n.116-116_116-115del
ENST00000668390.1:n.487-116_487-115del
ENST00000669994.1:c.91-116_91-115del ENSP00000499311.1:n.91-116_91-115del
ENST00000671528.1:c.91-116_91-115del ENSP00000499652.1:n.91-116_91-115del
ENST00000371975.8:c.91-116_91-115del ENSP00000361043.4:n.91-116_91-115del
ENST00000442598.5:c.91-116_91-115del ENSP00000396113.1:n.91-116_91-115del
ENST00000463715.5:c.-482-116_-482-115del ENSP00000480207.1:n.-482-116_-482-115del
ENST00000469835.5:c.91-116_91-115del ENSP00000477172.1:n.91-116_91-115del
ENST00000487700.1:n.88-116_88-115del
ENST00000493032.5:c.-314-116_-314-115del ENSP00000479995.1:n.-314-116_-314-115del
ENST00000493985.5:c.-450-116_-450-115del ENSP00000479823.1:n.-450-116_-450-115del
NM_001142548.1:c.91-116_91-115del NP_001136020.1:n.91-116_91-115del
NM_003579.3:c.91-116_91-115del NP_003570.2:n.91-116_91-115del
XM_006710975.2:c.-450-116_-450-115del XP_006711038.1:n.-450-116_-450-115del
XM_006710975.3:c.-450-116_-450-115del XP_006711038.1:n.-450-116_-450-115del
NM_003579.4:c.91-116_91-115del MANE Select NP_003570.2:n.91-116_91-115del
NM_001370766.1:c.-450-116_-450-115del NP_001357695.1:n.-450-116_-450-115del
NM_001142548.2:c.91-116_91-115del NP_001136020.1:n.91-116_91-115del