Canonical Allele Identifier: CA350493211

Gene: XRCC5

Linked Data

• MyVariant Identifiers: chr2:g.216986784G>C (hg19) ; chr2:g.216122061G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216122061G>C , CM000664.2:g.216122061G>C	GRCh38
NC_000002.11:g.216986784G>C , CM000664.1:g.216986784G>C	GRCh37
NC_000002.10:g.216695029G>C	NCBI36
NG_029780.1:g.17765G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392132.7:c.492-1G>C MANE Select	ENSP00000375977.2:n.492-1G>C
ENST00000392132.6:c.492-1G>C	ENSP00000375977.2:n.492-1G>C
ENST00000392133.7:c.492-1G>C	ENSP00000375978.3:n.492-1G>C
ENST00000460284.5:n.1034-1G>C
NM_021141.3:c.492-1G>C	NP_066964.1:n.492-1G>C
NM_021141.4:c.492-1G>C MANE Select	NP_066964.1:n.492-1G>C