Canonical Allele Identifier: CA2674491720

Gene: XRCC4

Linked Data

• gnomAD v4: 5-83353099-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83353099T>C , CM000667.2:g.83353099T>C	GRCh38
NC_000005.9:g.82648918T>C , CM000667.1:g.82648918T>C	GRCh37
NC_000005.8:g.82684674T>C	NCBI36
NG_047086.1:g.280691T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396027.9:c.894-32T>C MANE Select	ENSP00000379344.4:n.894-32T>C
ENST00000282268.7:c.894-32T>C	ENSP00000282268.3:n.894-32T>C
ENST00000338635.10:c.894-26T>C	ENSP00000342011.6:n.894-26T>C
ENST00000396027.8:c.894-32T>C	ENSP00000379344.4:n.894-32T>C
ENST00000511817.1:c.894-26T>C	ENSP00000421491.1:n.894-26T>C
NM_003401.3:c.894-32T>C	NP_003392.1:n.894-32T>C
NM_022406.2:c.894-26T>C	NP_071801.1:n.894-26T>C
NM_022550.2:c.894-32T>C	NP_072044.1:n.894-32T>C
XM_005248595.1:c.894-26T>C	XP_005248652.1:n.894-26T>C
XM_011543626.1:c.894-26T>C	XP_011541928.1:n.894-26T>C
XM_011543629.1:c.234-26T>C	XP_011541931.1:n.234-26T>C
NM_001318012.1:c.894-26T>C	NP_001304941.1:n.894-26T>C
NM_003401.4:c.894-32T>C	NP_003392.1:n.894-32T>C
NM_022406.3:c.894-26T>C	NP_071801.1:n.894-26T>C
NM_022550.3:c.894-32T>C	NP_072044.1:n.894-32T>C
XM_017009827.2:c.894-17168T>C	XP_016865316.1:n.894-17168T>C
NM_001318012.2:c.894-26T>C	NP_001304941.1:n.894-26T>C
NM_003401.5:c.894-32T>C MANE Select	NP_003392.1:n.894-32T>C
NM_022406.4:c.894-26T>C	NP_071801.1:n.894-26T>C
NM_001318012.3:c.894-26T>C	NP_001304941.1:n.894-26T>C
NM_022406.5:c.894-26T>C	NP_071801.1:n.894-26T>C
NM_022550.4:c.894-32T>C	NP_072044.1:n.894-32T>C