Canonical Allele Identifier: CA2503912002

Gene: XRCC4

Linked Data

• gnomAD v4: 5-83353434-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83353434G>T , CM000667.2:g.83353434G>T	GRCh38
NC_000005.9:g.82649253G>T , CM000667.1:g.82649253G>T	GRCh37
NC_000005.8:g.82685009G>T	NCBI36
NG_047086.1:g.281026G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396027.9:c.*192G>T MANE Select	ENSP00000379344.4:n.*192G>T
ENST00000282268.7:c.*192G>T	ENSP00000282268.3:n.*192G>T
ENST00000338635.10:c.*192G>T	ENSP00000342011.6:n.*192G>T
ENST00000396027.8:c.*192G>T	ENSP00000379344.4:n.*192G>T
ENST00000511817.1:c.*192G>T	ENSP00000421491.1:n.*192G>T
NM_003401.3:c.*192G>T	NP_003392.1:n.*192G>T
NM_022406.2:c.*192G>T	NP_071801.1:n.*192G>T
NM_022550.2:c.*192G>T	NP_072044.1:n.*192G>T
XM_005248595.1:c.*192G>T	XP_005248652.1:n.*192G>T
XM_011543626.1:c.*192G>T	XP_011541928.1:n.*192G>T
XM_011543629.1:c.*192G>T	XP_011541931.1:n.*192G>T
NM_001318012.1:c.*192G>T	NP_001304941.1:n.*192G>T
NM_003401.4:c.*192G>T	NP_003392.1:n.*192G>T
NM_022406.3:c.*192G>T	NP_071801.1:n.*192G>T
NM_022550.3:c.*192G>T	NP_072044.1:n.*192G>T
XM_017009827.2:c.894-16833G>T	XP_016865316.1:n.894-16833G>T
NM_001318012.2:c.*192G>T	NP_001304941.1:n.*192G>T
NM_003401.5:c.*192G>T MANE Select	NP_003392.1:n.*192G>T
NM_022406.4:c.*192G>T	NP_071801.1:n.*192G>T
NM_001318012.3:c.*192G>T	NP_001304941.1:n.*192G>T
NM_022406.5:c.*192G>T	NP_071801.1:n.*192G>T
NM_022550.4:c.*192G>T	NP_072044.1:n.*192G>T