Canonical Allele Identifier: CA834164
Gene: RAD54L HGNC NCBI

Linked Data

dbSNP Id: rs764062401
gnomAD v2: 1-46715789-C-T
gnomAD v3: 1-46250117-C-T
gnomAD v4: 1-46250117-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46250117C>T , CM000663.2:g.46250117C>T GRCh38
NC_000001.10:g.46715789C>T , CM000663.1:g.46715789C>T GRCh37
NC_000001.9:g.46488376C>T NCBI36
NG_012144.1:g.7423C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371975.9:c.208C>T MANE Select ENSP00000361043.4:p.His70Tyr
ENST00000469835.6:c.208C>T ENSP00000477172.2:p.His70Tyr
ENST00000655446.1:c.208C>T ENSP00000499451.1:p.His70Tyr
ENST00000657122.1:c.*110C>T ENSP00000499519.1:n.*110C>T
ENST00000669994.1:c.208C>T ENSP00000499311.1:p.His70Tyr
ENST00000671528.1:c.208C>T ENSP00000499652.1:p.His70Tyr
ENST00000371975.8:c.208C>T ENSP00000361043.4:p.His70Tyr
ENST00000442598.5:c.208C>T ENSP00000396113.1:p.His70Tyr
ENST00000463715.5:c.-365C>T ENSP00000480207.1:n.-365C>T
ENST00000469835.5:c.208C>T ENSP00000477172.1:p.His70Tyr
ENST00000487700.1:n.205C>T
ENST00000493032.5:c.-197C>T ENSP00000479995.1:n.-197C>T
ENST00000493985.5:c.-333C>T ENSP00000479823.1:n.-333C>T
NM_001142548.1:c.208C>T NP_001136020.1:p.His70Tyr
NM_003579.3:c.208C>T NP_003570.2:p.His70Tyr
XM_006710975.2:c.-333C>T XP_006711038.1:n.-333C>T
XM_006710975.3:c.-333C>T XP_006711038.1:n.-333C>T
NM_003579.4:c.208C>T MANE Select NP_003570.2:p.His70Tyr
NM_001370766.1:c.-333C>T NP_001357695.1:n.-333C>T
NM_001142548.2:c.208C>T NP_001136020.1:p.His70Tyr