Canonical Allele Identifier: CA400349119

Gene: RAD51C

Linked Data

• MyVariant Identifiers: chr17:g.56780572T>C (hg19) ; chr17:g.58703211T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703211T>C , CM000679.2:g.58703211T>C	GRCh38
NC_000017.10:g.56780572T>C , CM000679.1:g.56780572T>C	GRCh37
NC_000017.9:g.54135571T>C	NCBI36
NG_023199.1:g.15610T>C , LRG_314:g.15610T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.236T>C	ENSP00000464056.2:p.Leu79Ser
ENST00000697677.1:n.1668T>C
ENST00000697678.1:n.489T>C
ENST00000697679.1:n.1661T>C
ENST00000697680.1:c.*1451T>C	ENSP00000513392.1:n.*1451T>C
ENST00000697681.1:c.*1603T>C	ENSP00000513393.1:n.*1603T>C
ENST00000697683.1:c.*1451T>C	ENSP00000513395.1:n.*1451T>C
ENST00000697684.1:n.647T>C
ENST00000697685.1:c.*1284T>C	ENSP00000513396.1:n.*1284T>C
ENST00000697686.1:c.236T>C	ENSP00000513397.1:p.Leu79Ser
ENST00000697687.1:n.466T>C
ENST00000697688.1:n.633T>C
ENST00000697689.1:c.*1123T>C	ENSP00000513398.1:n.*1123T>C
ENST00000697690.1:c.587T>C	ENSP00000513399.1:p.Leu196Ser
ENST00000697691.1:c.*559T>C	ENSP00000513400.1:n.*559T>C
ENST00000697692.1:c.*599T>C	ENSP00000513401.1:n.*599T>C
ENST00000697694.1:c.236T>C	ENSP00000513402.1:p.Leu79Ser
ENST00000697695.1:n.1194T>C
ENST00000337432.9:c.587T>C MANE Select	ENSP00000336701.4:p.Leu196Ser
ENST00000337432.8:c.587T>C	ENSP00000336701.4:p.Leu196Ser
ENST00000413590.5:c.225T>C
ENST00000425173.5:c.383T>C	ENSP00000407282.1:p.Leu128Ser
ENST00000461271.5:c.236T>C	ENSP00000464056.1:p.Leu79Ser
ENST00000475762.5:c.*1290T>C	ENSP00000432421.1:n.*1290T>C
ENST00000482007.5:c.*15T>C	ENSP00000433332.1:n.*15T>C
ENST00000487525.5:c.*15T>C	ENSP00000431637.1:n.*15T>C
ENST00000487921.5:n.499T>C
ENST00000583539.5:c.587T>C	ENSP00000463121.1:p.Leu196Ser
ENST00000584617.5:c.309T>C
NM_058216.2:c.587T>C	NP_478123.1:p.Leu196Ser
NR_103872.1:n.491T>C
XM_006722001.2:c.587T>C	XP_006722064.1:p.Leu196Ser
XM_006722002.2:c.587T>C	XP_006722065.1:p.Leu196Ser
XM_006722004.2:c.236T>C	XP_006722067.1:p.Leu79Ser
XM_006722005.2:c.236T>C	XP_006722068.1:p.Leu79Ser
XM_011525092.1:c.236T>C	XP_011523394.1:p.Leu79Ser
XM_011525093.1:c.236T>C	XP_011523395.1:p.Leu79Ser
XM_011525094.1:c.236T>C	XP_011523396.1:p.Leu79Ser
XR_934513.1:n.660T>C
XR_934514.1:n.660T>C
XM_006722001.4:c.587T>C	XP_006722064.1:p.Leu196Ser
XM_006722002.4:c.587T>C	XP_006722065.1:p.Leu196Ser
XM_006722004.3:c.236T>C	XP_006722067.1:p.Leu79Ser
XM_006722005.3:c.236T>C	XP_006722068.1:p.Leu79Ser
XM_011525092.2:c.236T>C	XP_011523394.1:p.Leu79Ser
XM_011525093.2:c.236T>C	XP_011523395.1:p.Leu79Ser
XM_011525094.2:c.236T>C	XP_011523396.1:p.Leu79Ser
XM_017024914.1:c.236T>C	XP_016880403.1:p.Leu79Ser
XM_017024915.1:c.236T>C	XP_016880404.1:p.Leu79Ser
XM_017024916.1:c.236T>C	XP_016880405.1:p.Leu79Ser
XM_017024917.1:c.236T>C	XP_016880406.1:p.Leu79Ser
XM_017024918.2:c.236T>C	XP_016880407.1:p.Leu79Ser
XM_017024919.1:c.236T>C	XP_016880408.1:p.Leu79Ser
XR_934513.3:n.1091T>C
XR_934514.3:n.1091T>C
NM_058216.3:c.587T>C MANE Select	NP_478123.1:p.Leu196Ser
NR_103872.2:n.462T>C