Canonical Allele Identifier: CA400350172

Gene: RAD51C

Linked Data

• MyVariant Identifiers: chr17:g.56780689A>T (hg19) ; chr17:g.58703328A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703328A>T , CM000679.2:g.58703328A>T	GRCh38
NC_000017.10:g.56780689A>T , CM000679.1:g.56780689A>T	GRCh37
NC_000017.9:g.54135688A>T	NCBI36
NG_023199.1:g.15727A>T , LRG_314:g.15727A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.353A>T	ENSP00000464056.2:p.Lys118Met
ENST00000697677.1:n.1785A>T
ENST00000697678.1:n.606A>T
ENST00000697679.1:n.1778A>T
ENST00000697680.1:c.*1568A>T	ENSP00000513392.1:n.*1568A>T
ENST00000697681.1:c.*1720A>T	ENSP00000513393.1:n.*1720A>T
ENST00000697683.1:c.*1568A>T	ENSP00000513395.1:n.*1568A>T
ENST00000697684.1:n.764A>T
ENST00000697685.1:c.*1401A>T	ENSP00000513396.1:n.*1401A>T
ENST00000697686.1:c.353A>T	ENSP00000513397.1:p.Lys118Met
ENST00000697687.1:n.583A>T
ENST00000697688.1:n.750A>T
ENST00000697689.1:c.*1240A>T	ENSP00000513398.1:n.*1240A>T
ENST00000697690.1:c.704A>T	ENSP00000513399.1:p.Lys235Met
ENST00000697691.1:c.*676A>T	ENSP00000513400.1:n.*676A>T
ENST00000697692.1:c.*716A>T	ENSP00000513401.1:n.*716A>T
ENST00000697694.1:c.353A>T	ENSP00000513402.1:p.Lys118Met
ENST00000697695.1:n.1311A>T
ENST00000337432.9:c.704A>T MANE Select	ENSP00000336701.4:p.Lys235Met
ENST00000337432.8:c.704A>T	ENSP00000336701.4:p.Lys235Met
ENST00000413590.5:c.342A>T
ENST00000425173.5:c.500A>T	ENSP00000407282.1:p.Lys167Met
ENST00000461271.5:c.353A>T	ENSP00000464056.1:p.Lys118Met
ENST00000475762.5:c.*1407A>T	ENSP00000432421.1:n.*1407A>T
ENST00000482007.5:c.*132A>T	ENSP00000433332.1:n.*132A>T
ENST00000487525.5:c.*132A>T	ENSP00000431637.1:n.*132A>T
ENST00000487921.5:n.616A>T
ENST00000583539.5:c.704A>T	ENSP00000463121.1:p.Lys235Met
ENST00000584617.5:c.426A>T
NM_058216.2:c.704A>T	NP_478123.1:p.Lys235Met
NR_103872.1:n.608A>T
XM_006722001.2:c.704A>T	XP_006722064.1:p.Lys235Met
XM_006722002.2:c.704A>T	XP_006722065.1:p.Lys235Met
XM_006722004.2:c.353A>T	XP_006722067.1:p.Lys118Met
XM_006722005.2:c.353A>T	XP_006722068.1:p.Lys118Met
XM_011525092.1:c.353A>T	XP_011523394.1:p.Lys118Met
XM_011525093.1:c.353A>T	XP_011523395.1:p.Lys118Met
XM_011525094.1:c.353A>T	XP_011523396.1:p.Lys118Met
XR_934513.1:n.777A>T
XR_934514.1:n.777A>T
XM_006722001.4:c.704A>T	XP_006722064.1:p.Lys235Met
XM_006722002.4:c.704A>T	XP_006722065.1:p.Lys235Met
XM_006722004.3:c.353A>T	XP_006722067.1:p.Lys118Met
XM_006722005.3:c.353A>T	XP_006722068.1:p.Lys118Met
XM_011525092.2:c.353A>T	XP_011523394.1:p.Lys118Met
XM_011525093.2:c.353A>T	XP_011523395.1:p.Lys118Met
XM_011525094.2:c.353A>T	XP_011523396.1:p.Lys118Met
XM_017024914.1:c.353A>T	XP_016880403.1:p.Lys118Met
XM_017024915.1:c.353A>T	XP_016880404.1:p.Lys118Met
XM_017024916.1:c.353A>T	XP_016880405.1:p.Lys118Met
XM_017024917.1:c.353A>T	XP_016880406.1:p.Lys118Met
XM_017024918.2:c.353A>T	XP_016880407.1:p.Lys118Met
XM_017024919.1:c.353A>T	XP_016880408.1:p.Lys118Met
XR_934513.3:n.1208A>T
XR_934514.3:n.1208A>T
NM_058216.3:c.704A>T MANE Select	NP_478123.1:p.Lys235Met
NR_103872.2:n.579A>T