Canonical Allele Identifier: CA16499545
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.103704128G>A , CM000676.2:g.103704128G>A GRCh38
NC_000014.8:g.104170465G>A , CM000676.1:g.104170465G>A GRCh37
NC_000014.7:g.103240218G>A NCBI36
NG_011516.1:g.16359C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000555055.6:c.407-801C>T (XRCC3) MANE Select ENSP00000452598.1:n.407-801C>T
ENST00000348520.10:c.*2929G>A (KLC1) ENSP00000341154.6:n.*2929G>A
ENST00000352127.11:c.407-801C>T (XRCC3) ENSP00000343392.7:n.407-801C>T
ENST00000553264.5:c.407-801C>T (XRCC3) ENSP00000451974.1:n.407-801C>T
ENST00000553807.1:n.519-801C>T (XRCC3)
ENST00000554811.5:n.1854-801C>T (XRCC3)
ENST00000554913.5:c.407-801C>T (XRCC3) ENSP00000451362.1:n.407-801C>T
ENST00000554974.5:c.-54-4552C>T (XRCC3) ENSP00000451361.1:n.-54-4552C>T
ENST00000555055.5:c.407-801C>T (XRCC3) ENSP00000452598.1:n.407-801C>T
NM_001100118.1:c.407-801C>T (XRCC3) NP_001093588.1:n.407-801C>T
NM_001100119.1:c.407-801C>T (XRCC3) NP_001093589.1:n.407-801C>T
NM_005432.3:c.407-801C>T (XRCC3) NP_005423.1:n.407-801C>T
XM_005268046.1:c.407-801C>T (XRCC3) XP_005268103.1:n.407-801C>T
XM_011537138.1:c.407-801C>T (XRCC3) XP_011535440.1:n.407-801C>T
XM_005268046.2:c.407-801C>T (XRCC3) XP_005268103.1:n.407-801C>T
XM_011537138.2:c.407-801C>T (XRCC3) XP_011535440.1:n.407-801C>T
XM_024449799.1:c.345G>A XP_024305567.1:p.Lys115=
XM_024449800.1:c.258G>A XP_024305568.1:p.Lys86=
XR_002957596.1:n.613G>A
XR_002957597.1:n.682G>A
XR_002957598.1:n.501G>A
XR_002957599.1:n.249G>A
XR_002957600.1:n.402G>A
NM_005432.4:c.407-801C>T (XRCC3) MANE Select NP_005423.1:n.407-801C>T
NM_001100118.2:c.407-801C>T (XRCC3) NP_001093588.1:n.407-801C>T
NM_001100119.2:c.407-801C>T (XRCC3) NP_001093589.1:n.407-801C>T
NM_001371229.1:c.407-801C>T (XRCC3) NP_001358158.1:n.407-801C>T
NM_001371231.1:c.407-801C>T (XRCC3) NP_001358160.1:n.407-801C>T
NM_001371232.1:c.407-801C>T (XRCC3) NP_001358161.1:n.407-801C>T