Canonical Allele Identifier: CA3261179690
Community Standard Title: NM_058216.3(RAD51C):c.1036_1038delinsCTG (p.Phe346Leu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734127_58734129delinsCTG , CM000679.2:g.58734127_58734129delinsCTG GRCh38
NC_000017.10:g.56811488_56811490delinsCTG , CM000679.1:g.56811488_56811490delinsCTG GRCh37
NC_000017.9:g.54166487_54166489delinsCTG NCBI36
NG_023199.1:g.46526_46528delinsCTG , LRG_314:g.46526_46528delinsCTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1036_1038delinsCTG MANE Select NP_478123.1:p.Phe346Leu
ENST00000337432.9:c.1036_1038delinsCTG MANE Select ENSP00000336701.4:p.Phe346Leu
NM_058216.2:c.1036_1038delinsCTG NP_478123.1:p.Phe346Leu
NR_103872.1:n.940_942delinsCTG
NR_103872.2:n.911_913delinsCTG
ENST00000337432.8:c.1036_1038delinsCTG ENSP00000336701.4:p.Phe346Leu
ENST00000413590.5:c.677_679delinsCTG
ENST00000461271.6:c.*1568_*1570delinsCTG ENSP00000464056.2:n.*1568_*1570delinsCTG
ENST00000461706.1:n.223_225delinsCTG
ENST00000475762.5:c.*1672_*1674delinsCTG ENSP00000432421.1:n.*1672_*1674delinsCTG
ENST00000482007.5:c.*464_*466delinsCTG ENSP00000433332.1:n.*464_*466delinsCTG
ENST00000487525.5:c.*612_*614delinsCTG ENSP00000431637.1:n.*612_*614delinsCTG
ENST00000578151.1:n.249_251delinsCTG
ENST00000581221.5:n.551_553delinsCTG
ENST00000584804.1:c.270_272delinsCTG ENSP00000463658.1:p.Asp91Ter
ENST00000697680.1:c.*2000_*2002delinsCTG ENSP00000513392.1:n.*2000_*2002delinsCTG
ENST00000697681.1:c.*2197_*2199delinsCTG ENSP00000513393.1:n.*2197_*2199delinsCTG
ENST00000697683.1:c.*1972_*1974delinsCTG ENSP00000513395.1:n.*1972_*1974delinsCTG
ENST00000697685.1:c.*1733_*1735delinsCTG ENSP00000513396.1:n.*1733_*1735delinsCTG
ENST00000697686.1:c.807_809delinsCTG ENSP00000513397.1:p.Asp270Ter
ENST00000697689.1:c.*1450_*1452delinsCTG ENSP00000513398.1:n.*1450_*1452delinsCTG
ENST00000697690.1:c.914_916delinsCTG ENSP00000513399.1:p.Ile305_Ter306delinsThrGlu
ENST00000697691.1:c.*1008_*1010delinsCTG ENSP00000513400.1:n.*1008_*1010delinsCTG
ENST00000697692.1:c.*1048_*1050delinsCTG ENSP00000513401.1:n.*1048_*1050delinsCTG
ENST00000697694.1:c.685_687delinsCTG ENSP00000513402.1:p.Phe229Leu
ENST00000697695.1:n.1643_1645delinsCTG
XM_006722001.2:c.1039_1041delinsCTG XP_006722064.1:p.Phe347Leu
XM_006722001.4:c.1039_1041delinsCTG XP_006722064.1:p.Phe347Leu
XM_006722002.2:c.975_977delinsCTG XP_006722065.1:p.Asp326Ter
XM_006722002.4:c.975_977delinsCTG XP_006722065.1:p.Asp326Ter
XM_006722004.2:c.688_690delinsCTG XP_006722067.1:p.Phe230Leu
XM_006722004.3:c.688_690delinsCTG XP_006722067.1:p.Phe230Leu
XM_006722005.2:c.688_690delinsCTG XP_006722068.1:p.Phe230Leu
XM_006722005.3:c.688_690delinsCTG XP_006722068.1:p.Phe230Leu
XM_011525092.1:c.688_690delinsCTG XP_011523394.1:p.Phe230Leu
XM_011525092.2:c.688_690delinsCTG XP_011523394.1:p.Phe230Leu
XM_011525093.1:c.688_690delinsCTG XP_011523395.1:p.Phe230Leu
XM_011525093.2:c.688_690delinsCTG XP_011523395.1:p.Phe230Leu
XM_011525094.1:c.688_690delinsCTG XP_011523396.1:p.Phe230Leu
XM_011525094.2:c.688_690delinsCTG XP_011523396.1:p.Phe230Leu
XM_017024914.1:c.685_687delinsCTG XP_016880403.1:p.Phe229Leu
XM_017024915.1:c.685_687delinsCTG XP_016880404.1:p.Phe229Leu
XM_017024916.1:c.685_687delinsCTG XP_016880405.1:p.Phe229Leu
XM_017024917.1:c.685_687delinsCTG XP_016880406.1:p.Phe229Leu
XM_017024918.2:c.685_687delinsCTG XP_016880407.1:p.Phe229Leu
XM_017024919.1:c.624_626delinsCTG XP_016880408.1:p.Asp209Ter
XR_934513.1:n.1254_1256delinsCTG
XR_934513.3:n.1685_1687delinsCTG
XR_934514.1:n.1257_1259delinsCTG
XR_934514.3:n.1688_1690delinsCTG
XR_934886.1:n.149+3942_149+3944delinsCAG
XR_934886.2:n.149+3942_149+3944delinsCAG