Canonical Allele Identifier: CA501075213

Gene: RAD51C

Linked Data

• dbSNP Id: rs2143798097
• MyVariant Identifiers: chr17:g.56780603T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703242T>A , CM000679.2:g.58703242T>A	GRCh38
NC_000017.10:g.56780603T>A , CM000679.1:g.56780603T>A	GRCh37
NC_000017.9:g.54135602T>A	NCBI36
NG_023199.1:g.15641T>A , LRG_314:g.15641T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.267T>A	ENSP00000464056.2:p.Ser89=
ENST00000697677.1:n.1699T>A
ENST00000697678.1:n.520T>A
ENST00000697679.1:n.1692T>A
ENST00000697680.1:c.*1482T>A	ENSP00000513392.1:n.*1482T>A
ENST00000697681.1:c.*1634T>A	ENSP00000513393.1:n.*1634T>A
ENST00000697683.1:c.*1482T>A	ENSP00000513395.1:n.*1482T>A
ENST00000697684.1:n.678T>A
ENST00000697685.1:c.*1315T>A	ENSP00000513396.1:n.*1315T>A
ENST00000697686.1:c.267T>A	ENSP00000513397.1:p.Ser89=
ENST00000697687.1:n.497T>A
ENST00000697688.1:n.664T>A
ENST00000697689.1:c.*1154T>A	ENSP00000513398.1:n.*1154T>A
ENST00000697690.1:c.618T>A	ENSP00000513399.1:p.Ser206=
ENST00000697691.1:c.*590T>A	ENSP00000513400.1:n.*590T>A
ENST00000697692.1:c.*630T>A	ENSP00000513401.1:n.*630T>A
ENST00000697694.1:c.267T>A	ENSP00000513402.1:p.Ser89=
ENST00000697695.1:n.1225T>A
ENST00000337432.9:c.618T>A MANE Select	ENSP00000336701.4:p.Ser206=
ENST00000337432.8:c.618T>A	ENSP00000336701.4:p.Ser206=
ENST00000413590.5:c.256T>A
ENST00000425173.5:c.414T>A	ENSP00000407282.1:p.Ser138=
ENST00000461271.5:c.267T>A	ENSP00000464056.1:p.Ser89=
ENST00000475762.5:c.*1321T>A	ENSP00000432421.1:n.*1321T>A
ENST00000482007.5:c.*46T>A	ENSP00000433332.1:n.*46T>A
ENST00000487525.5:c.*46T>A	ENSP00000431637.1:n.*46T>A
ENST00000487921.5:n.530T>A
ENST00000583539.5:c.618T>A	ENSP00000463121.1:p.Ser206=
ENST00000584617.5:c.340T>A
NM_058216.2:c.618T>A	NP_478123.1:p.Ser206=
NR_103872.1:n.522T>A
XM_006722001.2:c.618T>A	XP_006722064.1:p.Ser206=
XM_006722002.2:c.618T>A	XP_006722065.1:p.Ser206=
XM_006722004.2:c.267T>A	XP_006722067.1:p.Ser89=
XM_006722005.2:c.267T>A	XP_006722068.1:p.Ser89=
XM_011525092.1:c.267T>A	XP_011523394.1:p.Ser89=
XM_011525093.1:c.267T>A	XP_011523395.1:p.Ser89=
XM_011525094.1:c.267T>A	XP_011523396.1:p.Ser89=
XR_934513.1:n.691T>A
XR_934514.1:n.691T>A
XM_006722001.4:c.618T>A	XP_006722064.1:p.Ser206=
XM_006722002.4:c.618T>A	XP_006722065.1:p.Ser206=
XM_006722004.3:c.267T>A	XP_006722067.1:p.Ser89=
XM_006722005.3:c.267T>A	XP_006722068.1:p.Ser89=
XM_011525092.2:c.267T>A	XP_011523394.1:p.Ser89=
XM_011525093.2:c.267T>A	XP_011523395.1:p.Ser89=
XM_011525094.2:c.267T>A	XP_011523396.1:p.Ser89=
XM_017024914.1:c.267T>A	XP_016880403.1:p.Ser89=
XM_017024915.1:c.267T>A	XP_016880404.1:p.Ser89=
XM_017024916.1:c.267T>A	XP_016880405.1:p.Ser89=
XM_017024917.1:c.267T>A	XP_016880406.1:p.Ser89=
XM_017024918.2:c.267T>A	XP_016880407.1:p.Ser89=
XM_017024919.1:c.267T>A	XP_016880408.1:p.Ser89=
XR_934513.3:n.1122T>A
XR_934514.3:n.1122T>A
NM_058216.3:c.618T>A MANE Select	NP_478123.1:p.Ser206=
NR_103872.2:n.493T>A