Canonical Allele Identifier: CA3261178752
Community Standard Title: NM_058216.3(RAD51C):c.17_18delinsAT (p.Phe6Tyr)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692660_58692661delinsAT , CM000679.2:g.58692660_58692661delinsAT GRCh38
NC_000017.10:g.56770021_56770022delinsAT , CM000679.1:g.56770021_56770022delinsAT GRCh37
NC_000017.9:g.54125020_54125021delinsAT NCBI36
NG_023199.1:g.5059_5060delinsAT , LRG_314:g.5059_5060delinsAT
NG_047169.1:g.4419_4420delinsAT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.17_18delinsAT MANE Select NP_478123.1:p.Phe6Tyr
ENST00000337432.9:c.17_18delinsAT MANE Select ENSP00000336701.4:p.Phe6Tyr
NM_002876.3:c.17_18delinsAT NP_002867.1:p.Phe6Tyr
NM_002876.4:c.17_18delinsAT NP_002867.1:p.Phe6Tyr
NM_058216.2:c.17_18delinsAT NP_478123.1:p.Phe6Tyr
NR_103872.1:n.88_89delinsAT
NR_103872.2:n.59_60delinsAT
NR_103873.1:n.88_89delinsAT
ENST00000337432.8:c.17_18delinsAT ENSP00000336701.4:p.Phe6Tyr
ENST00000421782.3:c.17_18delinsAT ENSP00000391450.2:p.Phe6Tyr
ENST00000461271.5:c.-232_-231delinsAT ENSP00000464056.1:n.-232_-231delinsAT
ENST00000461271.6:c.-232_-231delinsAT ENSP00000464056.2:n.-232_-231delinsAT
ENST00000475762.5:c.17_18delinsAT ENSP00000432421.1:p.Phe6Tyr
ENST00000476741.2:n.59_60delinsAT
ENST00000482007.5:c.17_18delinsAT ENSP00000433332.1:p.Phe6Tyr
ENST00000486827.1:c.17_18delinsAT ENSP00000436761.1:p.Phe6Tyr
ENST00000487525.5:c.17_18delinsAT ENSP00000431637.1:p.Phe6Tyr
ENST00000487921.5:n.57+28_57+29delinsAT
ENST00000583539.5:c.17_18delinsAT ENSP00000463121.1:p.Phe6Tyr
ENST00000697675.1:n.88_89delinsAT
ENST00000697676.1:n.77_78delinsAT
ENST00000697677.1:n.75_76delinsAT
ENST00000697678.1:n.47+28_47+29delinsAT
ENST00000697679.1:n.68_69delinsAT
ENST00000697680.1:c.17_18delinsAT ENSP00000513392.1:p.Phe6Tyr
ENST00000697681.1:c.17_18delinsAT ENSP00000513393.1:p.Phe6Tyr
ENST00000697683.1:c.17_18delinsAT ENSP00000513395.1:p.Phe6Tyr
ENST00000697684.1:n.77_78delinsAT
ENST00000697685.1:c.17_18delinsAT ENSP00000513396.1:p.Phe6Tyr
ENST00000697686.1:c.-207+28_-207+29delinsAT ENSP00000513397.1:n.-207+28_-207+29delinsAT
ENST00000697687.1:n.63_64delinsAT
ENST00000697688.1:n.63_64delinsAT
ENST00000697689.1:c.17_18delinsAT ENSP00000513398.1:p.Phe6Tyr
ENST00000697690.1:c.17_18delinsAT ENSP00000513399.1:p.Phe6Tyr
ENST00000697691.1:c.17_18delinsAT ENSP00000513400.1:p.Phe6Tyr
ENST00000697692.1:c.17_18delinsAT ENSP00000513401.1:p.Phe6Tyr
XM_006722001.2:c.17_18delinsAT XP_006722064.1:p.Phe6Tyr
XM_006722001.4:c.17_18delinsAT XP_006722064.1:p.Phe6Tyr
XM_006722002.2:c.17_18delinsAT XP_006722065.1:p.Phe6Tyr
XM_006722002.4:c.17_18delinsAT XP_006722065.1:p.Phe6Tyr
XM_006722004.2:c.-232_-231delinsAT XP_006722067.1:n.-232_-231delinsAT
XM_006722004.3:c.-232_-231delinsAT XP_006722067.1:n.-232_-231delinsAT
XM_006722005.2:c.-207+28_-207+29delinsAT XP_006722068.1:n.-207+28_-207+29delinsAT
XM_006722005.3:c.-207+28_-207+29delinsAT XP_006722068.1:n.-207+28_-207+29delinsAT
XM_011525092.1:c.-532_-531delinsAT XP_011523394.1:n.-532_-531delinsAT
XM_011525093.1:c.-693_-692delinsAT XP_011523395.1:n.-693_-692delinsAT
XM_017024914.1:c.-232_-231delinsAT XP_016880403.1:n.-232_-231delinsAT
XM_017024916.1:c.-532_-531delinsAT XP_016880405.1:n.-532_-531delinsAT
XM_017024917.1:c.-207+28_-207+29delinsAT XP_016880406.1:n.-207+28_-207+29delinsAT
XM_017024918.2:c.-506_-505delinsAT XP_016880407.1:n.-506_-505delinsAT
XR_934513.1:n.90_91delinsAT
XR_934513.3:n.521_522delinsAT
XR_934514.1:n.90_91delinsAT
XR_934514.3:n.521_522delinsAT