Canonical Allele Identifier: CA400364863
Community Standard Title: NM_058216.3(RAD51C):c.973A>G (p.Thr325Ala)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732491A>G , CM000679.2:g.58732491A>G GRCh38
NC_000017.10:g.56809852A>G , CM000679.1:g.56809852A>G GRCh37
NC_000017.9:g.54164851A>G NCBI36
NG_023199.1:g.44890A>G , LRG_314:g.44890A>G

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.973A>G MANE Select NP_478123.1:p.Thr325Ala
ENST00000337432.9:c.973A>G MANE Select ENSP00000336701.4:p.Thr325Ala
NM_058216.2:c.973A>G NP_478123.1:p.Thr325Ala
NR_103872.1:n.877A>G
NR_103872.2:n.848A>G
ENST00000337432.8:c.973A>G ENSP00000336701.4:p.Thr325Ala
ENST00000413590.5:c.614A>G
ENST00000461271.6:c.622A>G ENSP00000464056.2:p.Thr208Ala
ENST00000461706.1:n.160A>G
ENST00000475762.5:c.*1609A>G ENSP00000432421.1:n.*1609A>G
ENST00000482007.5:c.*401A>G ENSP00000433332.1:n.*401A>G
ENST00000487525.5:c.*549A>G ENSP00000431637.1:n.*549A>G
ENST00000578151.1:n.240-1627A>G
ENST00000581221.5:n.488A>G
ENST00000583539.5:c.973A>G ENSP00000463121.1:p.Thr325Ala
ENST00000584617.5:c.695A>G
ENST00000584804.1:c.207A>G ENSP00000463658.1:p.Gln69=
ENST00000697680.1:c.*1937A>G ENSP00000513392.1:n.*1937A>G
ENST00000697681.1:c.*2134A>G ENSP00000513393.1:n.*2134A>G
ENST00000697683.1:c.*1909A>G ENSP00000513395.1:n.*1909A>G
ENST00000697685.1:c.*1670A>G ENSP00000513396.1:n.*1670A>G
ENST00000697686.1:c.744A>G ENSP00000513397.1:p.Gln248=
ENST00000697689.1:c.*1441-1627A>G ENSP00000513398.1:n.*1441-1627A>G
ENST00000697690.1:c.905-1627A>G ENSP00000513399.1:n.905-1627A>G
ENST00000697691.1:c.*945A>G ENSP00000513400.1:n.*945A>G
ENST00000697692.1:c.*985A>G ENSP00000513401.1:n.*985A>G
ENST00000697694.1:c.622A>G ENSP00000513402.1:p.Thr208Ala
ENST00000697695.1:n.1580A>G
XM_006722001.2:c.976A>G XP_006722064.1:p.Thr326Ala
XM_006722001.4:c.976A>G XP_006722064.1:p.Thr326Ala
XM_006722002.2:c.912A>G XP_006722065.1:p.Gln304=
XM_006722002.4:c.912A>G XP_006722065.1:p.Gln304=
XM_006722004.2:c.625A>G XP_006722067.1:p.Thr209Ala
XM_006722004.3:c.625A>G XP_006722067.1:p.Thr209Ala
XM_006722005.2:c.625A>G XP_006722068.1:p.Thr209Ala
XM_006722005.3:c.625A>G XP_006722068.1:p.Thr209Ala
XM_011525092.1:c.625A>G XP_011523394.1:p.Thr209Ala
XM_011525092.2:c.625A>G XP_011523394.1:p.Thr209Ala
XM_011525093.1:c.625A>G XP_011523395.1:p.Thr209Ala
XM_011525093.2:c.625A>G XP_011523395.1:p.Thr209Ala
XM_011525094.1:c.625A>G XP_011523396.1:p.Thr209Ala
XM_011525094.2:c.625A>G XP_011523396.1:p.Thr209Ala
XM_017024914.1:c.622A>G XP_016880403.1:p.Thr208Ala
XM_017024915.1:c.622A>G XP_016880404.1:p.Thr208Ala
XM_017024916.1:c.622A>G XP_016880405.1:p.Thr208Ala
XM_017024917.1:c.622A>G XP_016880406.1:p.Thr208Ala
XM_017024918.2:c.622A>G XP_016880407.1:p.Thr208Ala
XM_017024919.1:c.561A>G XP_016880408.1:p.Gln187=
XR_934513.1:n.1191A>G
XR_934513.3:n.1622A>G
XR_934514.1:n.1194A>G
XR_934514.3:n.1625A>G
XR_934886.1:n.149+5580T>C
XR_934886.2:n.149+5580T>C