Canonical Allele Identifier: CA21908397

Gene: RAD54L LRRC41

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46267664G>C , CM000663.2:g.46267664G>C	GRCh38
NC_000001.10:g.46733336G>C , CM000663.1:g.46733336G>C	GRCh37
NC_000001.9:g.46505923G>C	NCBI36
NG_012144.1:g.24970G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371975.9:c.1042+55G>C (RAD54L) MANE Select	ENSP00000361043.4:n.1042+55G>C
ENST00000655446.1:c.*710+55G>C (RAD54L)	ENSP00000499451.1:n.*710+55G>C
ENST00000664182.1:n.105+55G>C (RAD54L)
ENST00000671528.1:c.1042+55G>C (RAD54L)	ENSP00000499652.1:n.1042+55G>C
ENST00000371975.8:c.1042+55G>C (RAD54L)	ENSP00000361043.4:n.1042+55G>C
ENST00000442598.5:c.1042+55G>C (RAD54L)	ENSP00000396113.1:n.1042+55G>C
ENST00000473251.2:c.503+55G>C (RAD54L)
ENST00000476687.2:c.199+55G>C (RAD54L)	ENSP00000479734.1:n.199+55G>C
ENST00000496156.5:c.514C>G (LRRC41)	ENSP00000477909.1:p.Pro172Ala
NM_001142548.1:c.1042+55G>C (RAD54L)	NP_001136020.1:n.1042+55G>C
NM_003579.3:c.1042+55G>C (RAD54L)	NP_003570.2:n.1042+55G>C
XM_006710975.2:c.502+55G>C (RAD54L)	XP_006711038.1:n.502+55G>C
XM_011542299.1:c.268+55G>C (RAD54L)	XP_011540601.1:n.268+55G>C
XM_011542300.1:c.268+55G>C (RAD54L)	XP_011540602.1:n.268+55G>C
XM_006710975.3:c.502+55G>C (RAD54L)	XP_006711038.1:n.502+55G>C
XM_011542299.2:c.268+55G>C (RAD54L)	XP_011540601.1:n.268+55G>C
XM_011542300.3:c.268+55G>C (RAD54L)	XP_011540602.1:n.268+55G>C
NM_003579.4:c.1042+55G>C (RAD54L) MANE Select	NP_003570.2:n.1042+55G>C
NM_001370766.1:c.502+55G>C (RAD54L)	NP_001357695.1:n.502+55G>C
NM_001142548.2:c.1042+55G>C (RAD54L)	NP_001136020.1:n.1042+55G>C