Canonical Allele Identifier: CA445279249

Gene: XRCC4

Linked Data

• MyVariant Identifiers: chr5:g.82648953T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83353134T>A , CM000667.2:g.83353134T>A	GRCh38
NC_000005.9:g.82648953T>A , CM000667.1:g.82648953T>A	GRCh37
NC_000005.8:g.82684709T>A	NCBI36
NG_047086.1:g.280726T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396027.9:c.897T>A MANE Select	ENSP00000379344.4:p.Pro299=
ENST00000282268.7:c.897T>A	ENSP00000282268.3:p.Pro299=
ENST00000338635.10:c.903T>A	ENSP00000342011.6:p.Pro301=
ENST00000396027.8:c.897T>A	ENSP00000379344.4:p.Pro299=
ENST00000511817.1:c.903T>A	ENSP00000421491.1:p.Pro301=
NM_003401.3:c.897T>A	NP_003392.1:p.Pro299=
NM_022406.2:c.903T>A	NP_071801.1:p.Pro301=
NM_022550.2:c.897T>A	NP_072044.1:p.Pro299=
XM_005248595.1:c.903T>A	XP_005248652.1:p.Pro301=
XM_011543626.1:c.903T>A	XP_011541928.1:p.Pro301=
XM_011543629.1:c.243T>A	XP_011541931.1:p.Pro81=
NM_001318012.1:c.903T>A	NP_001304941.1:p.Pro301=
NM_003401.4:c.897T>A	NP_003392.1:p.Pro299=
NM_022406.3:c.903T>A	NP_071801.1:p.Pro301=
NM_022550.3:c.897T>A	NP_072044.1:p.Pro299=
XM_017009827.2:c.894-17133T>A	XP_016865316.1:n.894-17133T>A
NM_001318012.2:c.903T>A	NP_001304941.1:p.Pro301=
NM_003401.5:c.897T>A MANE Select	NP_003392.1:p.Pro299=
NM_022406.4:c.903T>A	NP_071801.1:p.Pro301=
NM_001318012.3:c.903T>A	NP_001304941.1:p.Pro301=
NM_022406.5:c.903T>A	NP_071801.1:p.Pro301=
NM_022550.4:c.897T>A	NP_072044.1:p.Pro299=