Canonical Allele Identifier: CA360357601

Gene: XRCC4

Linked Data

• dbSNP Id: rs1336200309
• MyVariant Identifiers: chr5:g.82648952C>G (hg19) ; chr5:g.83353133C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83353133C>G , CM000667.2:g.83353133C>G	GRCh38
NC_000005.9:g.82648952C>G , CM000667.1:g.82648952C>G	GRCh37
NC_000005.8:g.82684708C>G	NCBI36
NG_047086.1:g.280725C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396027.9:c.896C>G MANE Select	ENSP00000379344.4:p.Pro299Arg
ENST00000282268.7:c.896C>G	ENSP00000282268.3:p.Pro299Arg
ENST00000338635.10:c.902C>G	ENSP00000342011.6:p.Pro301Arg
ENST00000396027.8:c.896C>G	ENSP00000379344.4:p.Pro299Arg
ENST00000511817.1:c.902C>G	ENSP00000421491.1:p.Pro301Arg
NM_003401.3:c.896C>G	NP_003392.1:p.Pro299Arg
NM_022406.2:c.902C>G	NP_071801.1:p.Pro301Arg
NM_022550.2:c.896C>G	NP_072044.1:p.Pro299Arg
XM_005248595.1:c.902C>G	XP_005248652.1:p.Pro301Arg
XM_011543626.1:c.902C>G	XP_011541928.1:p.Pro301Arg
XM_011543629.1:c.242C>G	XP_011541931.1:p.Pro81Arg
NM_001318012.1:c.902C>G	NP_001304941.1:p.Pro301Arg
NM_003401.4:c.896C>G	NP_003392.1:p.Pro299Arg
NM_022406.3:c.902C>G	NP_071801.1:p.Pro301Arg
NM_022550.3:c.896C>G	NP_072044.1:p.Pro299Arg
XM_017009827.2:c.894-17134C>G	XP_016865316.1:n.894-17134C>G
NM_001318012.2:c.902C>G	NP_001304941.1:p.Pro301Arg
NM_003401.5:c.896C>G MANE Select	NP_003392.1:p.Pro299Arg
NM_022406.4:c.902C>G	NP_071801.1:p.Pro301Arg
NM_001318012.3:c.902C>G	NP_001304941.1:p.Pro301Arg
NM_022406.5:c.902C>G	NP_071801.1:p.Pro301Arg
NM_022550.4:c.896C>G	NP_072044.1:p.Pro299Arg