Canonical Allele Identifier: CA445279274

Gene: XRCC4

Linked Data

• gnomAD v4: 5-83353173-C-T
• COSMIC: COSM5541864 ; COSM5541865
• MyVariant Identifiers: chr5:g.82648992C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83353173C>T , CM000667.2:g.83353173C>T	GRCh38
NC_000005.9:g.82648992C>T , CM000667.1:g.82648992C>T	GRCh37
NC_000005.8:g.82684748C>T	NCBI36
NG_047086.1:g.280765C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396027.9:c.936C>T MANE Select	ENSP00000379344.4:p.Ile312=
ENST00000282268.7:c.936C>T	ENSP00000282268.3:p.Ile312=
ENST00000338635.10:c.942C>T	ENSP00000342011.6:p.Ile314=
ENST00000396027.8:c.936C>T	ENSP00000379344.4:p.Ile312=
ENST00000511817.1:c.942C>T	ENSP00000421491.1:p.Ile314=
NM_003401.3:c.936C>T	NP_003392.1:p.Ile312=
NM_022406.2:c.942C>T	NP_071801.1:p.Ile314=
NM_022550.2:c.936C>T	NP_072044.1:p.Ile312=
XM_005248595.1:c.942C>T	XP_005248652.1:p.Ile314=
XM_011543626.1:c.942C>T	XP_011541928.1:p.Ile314=
XM_011543629.1:c.282C>T	XP_011541931.1:p.Ile94=
NM_001318012.1:c.942C>T	NP_001304941.1:p.Ile314=
NM_003401.4:c.936C>T	NP_003392.1:p.Ile312=
NM_022406.3:c.942C>T	NP_071801.1:p.Ile314=
NM_022550.3:c.936C>T	NP_072044.1:p.Ile312=
XM_017009827.2:c.894-17094C>T	XP_016865316.1:n.894-17094C>T
NM_001318012.2:c.942C>T	NP_001304941.1:p.Ile314=
NM_003401.5:c.936C>T MANE Select	NP_003392.1:p.Ile312=
NM_022406.4:c.942C>T	NP_071801.1:p.Ile314=
NM_001318012.3:c.942C>T	NP_001304941.1:p.Ile314=
NM_022406.5:c.942C>T	NP_071801.1:p.Ile314=
NM_022550.4:c.936C>T	NP_072044.1:p.Ile312=