Canonical Allele Identifier: CA400354028

Gene: RAD51C

Linked Data

• MyVariant Identifiers: chr17:g.56787301A>T (hg19) ; chr17:g.58709940A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709940A>T , CM000679.2:g.58709940A>T	GRCh38
NC_000017.10:g.56787301A>T , CM000679.1:g.56787301A>T	GRCh37
NC_000017.9:g.54142300A>T	NCBI36
NG_023199.1:g.22339A>T , LRG_314:g.22339A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.436A>T	ENSP00000464056.2:p.Asn146Tyr
ENST00000697678.1:n.689A>T
ENST00000697679.1:n.1861A>T
ENST00000697680.1:c.*1651A>T	ENSP00000513392.1:n.*1651A>T
ENST00000697681.1:c.*1948A>T	ENSP00000513393.1:n.*1948A>T
ENST00000697683.1:c.*1651A>T	ENSP00000513395.1:n.*1651A>T
ENST00000697684.1:n.847A>T
ENST00000697685.1:c.*1484A>T	ENSP00000513396.1:n.*1484A>T
ENST00000697686.1:c.436A>T	ENSP00000513397.1:p.Asn146Tyr
ENST00000697687.1:n.666A>T
ENST00000697688.1:n.833A>T
ENST00000697689.1:c.*1323A>T	ENSP00000513398.1:n.*1323A>T
ENST00000697690.1:c.787A>T	ENSP00000513399.1:p.Asn263Tyr
ENST00000697691.1:c.*759A>T	ENSP00000513400.1:n.*759A>T
ENST00000697692.1:c.*799A>T	ENSP00000513401.1:n.*799A>T
ENST00000697694.1:c.436A>T	ENSP00000513402.1:p.Asn146Tyr
ENST00000697695.1:n.1394A>T
ENST00000337432.9:c.787A>T MANE Select	ENSP00000336701.4:p.Asn263Tyr
ENST00000337432.8:c.787A>T	ENSP00000336701.4:p.Asn263Tyr
ENST00000413590.5:c.425A>T
ENST00000475762.5:c.*1490A>T	ENSP00000432421.1:n.*1490A>T
ENST00000482007.5:c.*215A>T	ENSP00000433332.1:n.*215A>T
ENST00000487525.5:c.*360A>T	ENSP00000431637.1:n.*360A>T
ENST00000578151.1:n.122A>T
ENST00000581221.5:n.302A>T
ENST00000583539.5:c.787A>T	ENSP00000463121.1:p.Asn263Tyr
ENST00000584617.5:c.509A>T
ENST00000584804.1:c.82A>T	ENSP00000463658.1:p.Asn28Tyr
NM_058216.2:c.787A>T	NP_478123.1:p.Asn263Tyr
NR_103872.1:n.691A>T
XM_006722001.2:c.787A>T	XP_006722064.1:p.Asn263Tyr
XM_006722002.2:c.787A>T	XP_006722065.1:p.Asn263Tyr
XM_006722004.2:c.436A>T	XP_006722067.1:p.Asn146Tyr
XM_006722005.2:c.436A>T	XP_006722068.1:p.Asn146Tyr
XM_011525092.1:c.436A>T	XP_011523394.1:p.Asn146Tyr
XM_011525093.1:c.436A>T	XP_011523395.1:p.Asn146Tyr
XM_011525094.1:c.436A>T	XP_011523396.1:p.Asn146Tyr
XR_934513.1:n.1005A>T
XR_934514.1:n.1005A>T
XM_006722001.4:c.787A>T	XP_006722064.1:p.Asn263Tyr
XM_006722002.4:c.787A>T	XP_006722065.1:p.Asn263Tyr
XM_006722004.3:c.436A>T	XP_006722067.1:p.Asn146Tyr
XM_006722005.3:c.436A>T	XP_006722068.1:p.Asn146Tyr
XM_011525092.2:c.436A>T	XP_011523394.1:p.Asn146Tyr
XM_011525093.2:c.436A>T	XP_011523395.1:p.Asn146Tyr
XM_011525094.2:c.436A>T	XP_011523396.1:p.Asn146Tyr
XM_017024914.1:c.436A>T	XP_016880403.1:p.Asn146Tyr
XM_017024915.1:c.436A>T	XP_016880404.1:p.Asn146Tyr
XM_017024916.1:c.436A>T	XP_016880405.1:p.Asn146Tyr
XM_017024917.1:c.436A>T	XP_016880406.1:p.Asn146Tyr
XM_017024918.2:c.436A>T	XP_016880407.1:p.Asn146Tyr
XM_017024919.1:c.436A>T	XP_016880408.1:p.Asn146Tyr
XR_934513.3:n.1436A>T
XR_934514.3:n.1436A>T
NM_058216.3:c.787A>T MANE Select	NP_478123.1:p.Asn263Tyr
NR_103872.2:n.662A>T