Canonical Allele Identifier: CA340175315

Gene: RAD54L

Linked Data

• MyVariant Identifiers: chr1:g.46715672A>T (hg19) ; chr1:g.46250000A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46250000A>T , CM000663.2:g.46250000A>T	GRCh38
NC_000001.10:g.46715672A>T , CM000663.1:g.46715672A>T	GRCh37
NC_000001.9:g.46488259A>T	NCBI36
NG_012144.1:g.7306A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371975.9:c.91A>T MANE Select	ENSP00000361043.4:p.Thr31Ser
ENST00000469835.6:c.91A>T	ENSP00000477172.2:p.Thr31Ser
ENST00000655446.1:c.91A>T	ENSP00000499451.1:p.Thr31Ser
ENST00000657122.1:c.116A>T	ENSP00000499519.1:p.Asp39Val
ENST00000668390.1:n.487A>T
ENST00000669994.1:c.91A>T	ENSP00000499311.1:p.Thr31Ser
ENST00000671528.1:c.91A>T	ENSP00000499652.1:p.Thr31Ser
ENST00000371975.8:c.91A>T	ENSP00000361043.4:p.Thr31Ser
ENST00000442598.5:c.91A>T	ENSP00000396113.1:p.Thr31Ser
ENST00000463715.5:c.-482A>T	ENSP00000480207.1:n.-482A>T
ENST00000469835.5:c.91A>T	ENSP00000477172.1:p.Thr31Ser
ENST00000487700.1:n.88A>T
ENST00000493032.5:c.-314A>T	ENSP00000479995.1:n.-314A>T
ENST00000493985.5:c.-450A>T	ENSP00000479823.1:n.-450A>T
NM_001142548.1:c.91A>T	NP_001136020.1:p.Thr31Ser
NM_003579.3:c.91A>T	NP_003570.2:p.Thr31Ser
XM_006710975.2:c.-450A>T	XP_006711038.1:n.-450A>T
XM_006710975.3:c.-450A>T	XP_006711038.1:n.-450A>T
NM_003579.4:c.91A>T MANE Select	NP_003570.2:p.Thr31Ser
NM_001370766.1:c.-450A>T	NP_001357695.1:n.-450A>T
NM_001142548.2:c.91A>T	NP_001136020.1:p.Thr31Ser