Canonical Allele Identifier: CA2171911617

Gene: RAD51

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40718718_40718719delinsGA , CM000677.2:g.40718718_40718719delinsGA	GRCh38
NC_000015.9:g.41010916_41010917delinsGA , CM000677.1:g.41010916_41010917delinsGA	GRCh37
NC_000015.8:g.38798208_38798209delinsGA	NCBI36
NG_012120.1:g.28558_28559delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267868.8:c.436-87_436-86delinsGA MANE Select	ENSP00000267868.3:n.436-87_436-86delinsGA
ENST00000532743.6:c.436-87_436-86delinsGA	ENSP00000433924.2:n.436-87_436-86delinsGA
ENST00000645673.2:c.439-87_439-86delinsGA	ENSP00000493712.2:n.439-87_439-86delinsGA
ENST00000267868.7:c.436-87_436-86delinsGA	ENSP00000267868.3:n.436-87_436-86delinsGA
ENST00000382643.7:c.439-87_439-86delinsGA	ENSP00000372088.3:n.439-87_439-86delinsGA
ENST00000423169.6:c.436-87_436-86delinsGA	ENSP00000406602.2:n.436-87_436-86delinsGA
ENST00000525066.5:c.435+9602_435+9603delinsGA	ENSP00000431864.1:n.435+9602_435+9603delinsGA
ENST00000527860.5:c.436-87_436-86delinsGA	ENSP00000432759.1:n.436-87_436-86delinsGA
ENST00000531277.2:c.*15-87_*15-86delinsGA	ENSP00000436512.2:n.*15-87_*15-86delinsGA
ENST00000532743.5:c.439-87_439-86delinsGA	ENSP00000433924.1:n.439-87_439-86delinsGA
ENST00000533741.1:c.403-87_403-86delinsGA
ENST00000557850.5:c.226-168_226-167delinsGA	ENSP00000454176.1:n.226-168_226-167delinsGA
NM_001164269.1:c.439-87_439-86delinsGA	NP_001157741.1:n.439-87_439-86delinsGA
NM_001164270.1:c.436-87_436-86delinsGA	NP_001157742.1:n.436-87_436-86delinsGA
NM_002875.4:c.436-87_436-86delinsGA	NP_002866.2:n.436-87_436-86delinsGA
NM_133487.3:c.439-87_439-86delinsGA	NP_597994.3:n.439-87_439-86delinsGA
XM_006720626.2:c.436-87_436-86delinsGA	XP_006720689.1:n.436-87_436-86delinsGA
XM_011521857.1:c.436-87_436-86delinsGA	XP_011520159.1:n.436-87_436-86delinsGA
XM_011521858.1:c.436-87_436-86delinsGA	XP_011520160.1:n.436-87_436-86delinsGA
XM_011521859.1:c.436-87_436-86delinsGA	XP_011520161.1:n.436-87_436-86delinsGA
XM_011521860.1:c.436-87_436-86delinsGA	XP_011520162.1:n.436-87_436-86delinsGA
XM_011521861.1:c.436-87_436-86delinsGA	XP_011520163.1:n.436-87_436-86delinsGA
XM_011521862.1:c.64-87_64-86delinsGA	XP_011520164.1:n.64-87_64-86delinsGA
XM_006720626.3:c.436-87_436-86delinsGA	XP_006720689.1:n.436-87_436-86delinsGA
XM_011521857.2:c.436-87_436-86delinsGA	XP_011520159.1:n.436-87_436-86delinsGA
XM_011521858.2:c.436-87_436-86delinsGA	XP_011520160.1:n.436-87_436-86delinsGA
XM_011521859.2:c.436-87_436-86delinsGA	XP_011520161.1:n.436-87_436-86delinsGA
XM_011521860.2:c.436-87_436-86delinsGA	XP_011520162.1:n.436-87_436-86delinsGA
XM_011521861.2:c.436-87_436-86delinsGA	XP_011520163.1:n.436-87_436-86delinsGA
XM_011521862.3:c.64-87_64-86delinsGA	XP_011520164.1:n.64-87_64-86delinsGA
NM_001164269.2:c.439-87_439-86delinsGA	NP_001157741.1:n.439-87_439-86delinsGA
NM_001164270.2:c.436-87_436-86delinsGA	NP_001157742.1:n.436-87_436-86delinsGA
NM_002875.5:c.436-87_436-86delinsGA MANE Select	NP_002866.2:n.436-87_436-86delinsGA
NM_133487.4:c.439-87_439-86delinsGA	NP_597994.3:n.439-87_439-86delinsGA