Canonical Allele Identifier: CA13951441
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.103712930T>C , CM000676.2:g.103712930T>C GRCh38
NC_000014.8:g.104179267T>C , CM000676.1:g.104179267T>C GRCh37
NC_000014.7:g.103249020T>C NCBI36
NG_011516.1:g.7557A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000555055.6:c.-316A>G (XRCC3) MANE Select ENSP00000452598.1:n.-316A>G
ENST00000348520.10:c.*11731T>C (KLC1) ENSP00000341154.6:n.*11731T>C
ENST00000352127.11:c.-260-1363A>G (XRCC3) ENSP00000343392.7:n.-260-1363A>G
ENST00000553332.5:c.-354-1269A>G (XRCC3) ENSP00000450780.1:n.-354-1269A>G
ENST00000553361.5:c.-260-1363A>G (XRCC3) ENSP00000451118.1:n.-260-1363A>G
ENST00000554170.1:c.-316A>G (XRCC3) ENSP00000450738.1:n.-316A>G
ENST00000554913.5:c.-251A>G (XRCC3) ENSP00000451362.1:n.-251A>G
ENST00000554974.5:c.-55+2494A>G (XRCC3) ENSP00000451361.1:n.-55+2494A>G
ENST00000555055.5:c.-316A>G (XRCC3) ENSP00000452598.1:n.-316A>G
ENST00000555231.5:n.37-1363A>G (XRCC3)
ENST00000555964.5:c.-195-1363A>G (XRCC3) ENSP00000451173.1:n.-195-1363A>G
ENST00000556682.5:c.-289-1269A>G (XRCC3) ENSP00000452389.1:n.-289-1269A>G
ENST00000556980.5:c.-316A>G (XRCC3) ENSP00000451252.1:n.-316A>G
ENST00000557439.5:c.-316A>G (XRCC3) ENSP00000473569.1:n.-316A>G
NM_001100118.1:c.-260-1363A>G (XRCC3) NP_001093588.1:n.-260-1363A>G
NM_001100119.1:c.-316A>G (XRCC3) NP_001093589.1:n.-316A>G
NM_005432.3:c.-316A>G (XRCC3) NP_005423.1:n.-316A>G
XM_005268046.1:c.-354-1269A>G (XRCC3) XP_005268103.1:n.-354-1269A>G
XM_011537138.1:c.-316A>G (XRCC3) XP_011535440.1:n.-316A>G
XM_005268046.2:c.-354-1269A>G (XRCC3) XP_005268103.1:n.-354-1269A>G
XM_011537138.2:c.-316A>G (XRCC3) XP_011535440.1:n.-316A>G
NM_005432.4:c.-316A>G (XRCC3) MANE Select NP_005423.1:n.-316A>G
NM_001100118.2:c.-260-1363A>G (XRCC3) NP_001093588.1:n.-260-1363A>G
NM_001100119.2:c.-316A>G (XRCC3) NP_001093589.1:n.-316A>G
NM_001371229.1:c.-316A>G (XRCC3) NP_001358158.1:n.-316A>G
NM_001371231.1:c.-410A>G (XRCC3) NP_001358160.1:n.-410A>G
NM_001371232.1:c.-251A>G (XRCC3) NP_001358161.1:n.-251A>G