Canonical Allele Identifier: CA2638988612

Gene: RAD51C

Linked Data

• gnomAD v4: 17-58692576-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692576G>T , CM000679.2:g.58692576G>T	GRCh38
NC_000017.10:g.56769937G>T , CM000679.1:g.56769937G>T	GRCh37
NC_000017.9:g.54124936G>T	NCBI36
NG_023199.1:g.4975G>T , LRG_314:g.4975G>T
NG_047169.1:g.4504C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-316G>T	ENSP00000464056.2:n.-316G>T
ENST00000697675.1:n.4G>T
ENST00000337432.8:c.-68G>T	ENSP00000336701.4:n.-68G>T
ENST00000461271.5:c.-316G>T	ENSP00000464056.1:n.-316G>T
ENST00000487921.5:n.1G>T
ENST00000583539.5:c.-68G>T	ENSP00000463121.1:n.-68G>T
NM_002876.3:c.-68G>T	NP_002867.1:n.-68G>T
NM_058216.2:c.-68G>T	NP_478123.1:n.-68G>T
NR_103872.1:n.4G>T
NR_103873.1:n.4G>T
XM_006722001.2:c.-68G>T	XP_006722064.1:n.-68G>T
XM_006722002.2:c.-68G>T	XP_006722065.1:n.-68G>T
XM_006722004.2:c.-316G>T	XP_006722067.1:n.-316G>T
XM_006722005.2:c.-263G>T	XP_006722068.1:n.-263G>T
XR_934513.1:n.6G>T
XR_934514.1:n.6G>T
XM_006722001.4:c.-68G>T	XP_006722064.1:n.-68G>T
XM_006722002.4:c.-68G>T	XP_006722065.1:n.-68G>T
XM_006722005.3:c.-263G>T	XP_006722068.1:n.-263G>T
XM_017024917.1:c.-263G>T	XP_016880406.1:n.-263G>T
XR_934513.3:n.437G>T
XR_934514.3:n.437G>T