Canonical Allele Identifier: CA400364940
Community Standard Title: NM_058216.3(RAD51C):c.988C>T (p.Pro330Ser)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732506C>T , CM000679.2:g.58732506C>T GRCh38
NC_000017.10:g.56809867C>T , CM000679.1:g.56809867C>T GRCh37
NC_000017.9:g.54164866C>T NCBI36
NG_023199.1:g.44905C>T , LRG_314:g.44905C>T

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.988C>T MANE Select NP_478123.1:p.Pro330Ser
ENST00000337432.9:c.988C>T MANE Select ENSP00000336701.4:p.Pro330Ser
NM_058216.2:c.988C>T NP_478123.1:p.Pro330Ser
NR_103872.1:n.892C>T
NR_103872.2:n.863C>T
ENST00000337432.8:c.988C>T ENSP00000336701.4:p.Pro330Ser
ENST00000413590.5:c.629C>T
ENST00000461271.6:c.637C>T ENSP00000464056.2:p.Pro213Ser
ENST00000461706.1:n.175C>T
ENST00000475762.5:c.*1624C>T ENSP00000432421.1:n.*1624C>T
ENST00000482007.5:c.*416C>T ENSP00000433332.1:n.*416C>T
ENST00000487525.5:c.*564C>T ENSP00000431637.1:n.*564C>T
ENST00000578151.1:n.240-1612C>T
ENST00000581221.5:n.503C>T
ENST00000583539.5:c.988C>T ENSP00000463121.1:p.Pro330Ser
ENST00000584617.5:c.710C>T
ENST00000584804.1:c.222C>T ENSP00000463658.1:p.His74=
ENST00000697680.1:c.*1952C>T ENSP00000513392.1:n.*1952C>T
ENST00000697681.1:c.*2149C>T ENSP00000513393.1:n.*2149C>T
ENST00000697683.1:c.*1924C>T ENSP00000513395.1:n.*1924C>T
ENST00000697685.1:c.*1685C>T ENSP00000513396.1:n.*1685C>T
ENST00000697686.1:c.759C>T ENSP00000513397.1:p.His253=
ENST00000697689.1:c.*1441-1612C>T ENSP00000513398.1:n.*1441-1612C>T
ENST00000697690.1:c.905-1612C>T ENSP00000513399.1:n.905-1612C>T
ENST00000697691.1:c.*960C>T ENSP00000513400.1:n.*960C>T
ENST00000697692.1:c.*1000C>T ENSP00000513401.1:n.*1000C>T
ENST00000697694.1:c.637C>T ENSP00000513402.1:p.Pro213Ser
ENST00000697695.1:n.1595C>T
XM_006722001.2:c.991C>T XP_006722064.1:p.Pro331Ser
XM_006722001.4:c.991C>T XP_006722064.1:p.Pro331Ser
XM_006722002.2:c.927C>T XP_006722065.1:p.His309=
XM_006722002.4:c.927C>T XP_006722065.1:p.His309=
XM_006722004.2:c.640C>T XP_006722067.1:p.Pro214Ser
XM_006722004.3:c.640C>T XP_006722067.1:p.Pro214Ser
XM_006722005.2:c.640C>T XP_006722068.1:p.Pro214Ser
XM_006722005.3:c.640C>T XP_006722068.1:p.Pro214Ser
XM_011525092.1:c.640C>T XP_011523394.1:p.Pro214Ser
XM_011525092.2:c.640C>T XP_011523394.1:p.Pro214Ser
XM_011525093.1:c.640C>T XP_011523395.1:p.Pro214Ser
XM_011525093.2:c.640C>T XP_011523395.1:p.Pro214Ser
XM_011525094.1:c.640C>T XP_011523396.1:p.Pro214Ser
XM_011525094.2:c.640C>T XP_011523396.1:p.Pro214Ser
XM_017024914.1:c.637C>T XP_016880403.1:p.Pro213Ser
XM_017024915.1:c.637C>T XP_016880404.1:p.Pro213Ser
XM_017024916.1:c.637C>T XP_016880405.1:p.Pro213Ser
XM_017024917.1:c.637C>T XP_016880406.1:p.Pro213Ser
XM_017024918.2:c.637C>T XP_016880407.1:p.Pro213Ser
XM_017024919.1:c.576C>T XP_016880408.1:p.His192=
XR_934513.1:n.1206C>T
XR_934513.3:n.1637C>T
XR_934514.1:n.1209C>T
XR_934514.3:n.1640C>T
XR_934886.1:n.149+5565G>A
XR_934886.2:n.149+5565G>A