Canonical Allele Identifier: CA539838336

Gene: XRCC5

Linked Data

• dbSNP Id: rs1182716507
• gnomAD v2: 2-216986750-TTAGAA-T
• MyVariant Identifiers: chr2:g.216986751_216986755del (hg19) ; chr2:g.216122028_216122032del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216122028_216122032del , CM000664.2:g.216122028_216122032del	GRCh38
NC_000002.11:g.216986751_216986755del , CM000664.1:g.216986751_216986755del	GRCh37
NC_000002.10:g.216694996_216695000del	NCBI36
NG_029780.1:g.17732_17736del

Transcript Alleles

HGVS	Amino-acid change
ENST00000392132.7:c.492-34_492-30del MANE Select	ENSP00000375977.2:n.492-34_492-30del
ENST00000392132.6:c.492-34_492-30del	ENSP00000375977.2:n.492-34_492-30del
ENST00000392133.7:c.492-34_492-30del	ENSP00000375978.3:n.492-34_492-30del
ENST00000460284.5:n.1034-34_1034-30del
NM_021141.3:c.492-34_492-30del	NP_066964.1:n.492-34_492-30del
NM_021141.4:c.492-34_492-30del MANE Select	NP_066964.1:n.492-34_492-30del