Canonical Allele Identifier: CA2267813903
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692577T= , CM000679.2:g.58692577T= GRCh38
NC_000017.10:g.56769938T= , CM000679.1:g.56769938T= GRCh37
NC_000017.9:g.54124937T= NCBI36
NG_023199.1:g.4976T= , LRG_314:g.4976T=
NG_047169.1:g.4503A=

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.-315T= ENSP00000464056.2:n.-315T=
ENST00000697675.1:n.5T=
ENST00000337432.8:c.-67T= ENSP00000336701.4:n.-67T=
ENST00000461271.5:c.-315T= ENSP00000464056.1:n.-315T=
ENST00000487921.5:n.2T=
ENST00000583539.5:c.-67T= ENSP00000463121.1:n.-67T=
NM_002876.3:c.-67T= NP_002867.1:n.-67T=
NM_058216.2:c.-67T= NP_478123.1:n.-67T=
NR_103872.1:n.5T=
NR_103873.1:n.5T=
XM_006722001.2:c.-67T= XP_006722064.1:n.-67T=
XM_006722002.2:c.-67T= XP_006722065.1:n.-67T=
XM_006722004.2:c.-315T= XP_006722067.1:n.-315T=
XM_006722005.2:c.-262T= XP_006722068.1:n.-262T=
XR_934513.1:n.7T=
XR_934514.1:n.7T=
XM_006722001.4:c.-67T= XP_006722064.1:n.-67T=
XM_006722002.4:c.-67T= XP_006722065.1:n.-67T=
XM_006722004.3:c.-315T= XP_006722067.1:n.-315T=
XM_006722005.3:c.-262T= XP_006722068.1:n.-262T=
XM_017024914.1:c.-315T= XP_016880403.1:n.-315T=
XM_017024917.1:c.-262T= XP_016880406.1:n.-262T=
XR_934513.3:n.438T=
XR_934514.3:n.438T=