Canonical Allele Identifier: CA1327685877
Gene: XRCC5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216122020T= , CM000664.2:g.216122020T= GRCh38
NC_000002.11:g.216986743T= , CM000664.1:g.216986743T= GRCh37
NC_000002.10:g.216694988T= NCBI36
NG_029780.1:g.17724T=

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.492-42T= MANE Select ENSP00000375977.2:n.492-42T=
ENST00000392132.6:c.492-42T= ENSP00000375977.2:n.492-42T=
ENST00000392133.7:c.492-42T= ENSP00000375978.3:n.492-42T=
ENST00000460284.5:n.1034-42T=
NM_021141.3:c.492-42T= NP_066964.1:n.492-42T=
NM_021141.4:c.492-42T= MANE Select NP_066964.1:n.492-42T=
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