Canonical Allele Identifier: CA122028035

Gene: XRCC4

Linked Data

• dbSNP Id: rs7734849
• gnomAD v2: 5-82639949-T-A
• gnomAD v3: 5-83344130-T-A
• gnomAD v4: 5-83344130-T-A
• MyVariant Identifiers: chr5:g.82639949T>A (hg19) ; chr5:g.82639949_82639953delinsACACA (hg19) ; chr5:g.83344130T>A (hg38) ; chr5:g.83344130_83344134delinsACACA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.83344130T>A , CM000667.2:g.83344130T>A	GRCh38
NC_000005.9:g.82639949T>A , CM000667.1:g.82639949T>A	GRCh37
NC_000005.8:g.82675705T>A	NCBI36
NG_047086.1:g.271722T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396027.9:c.894-9001T>A MANE Select	ENSP00000379344.4:n.894-9001T>A
ENST00000282268.7:c.894-9001T>A	ENSP00000282268.3:n.894-9001T>A
ENST00000338635.10:c.894-8995T>A	ENSP00000342011.6:n.894-8995T>A
ENST00000396027.8:c.894-9001T>A	ENSP00000379344.4:n.894-9001T>A
ENST00000511817.1:c.894-8995T>A	ENSP00000421491.1:n.894-8995T>A
NM_003401.3:c.894-9001T>A	NP_003392.1:n.894-9001T>A
NM_022406.2:c.894-8995T>A	NP_071801.1:n.894-8995T>A
NM_022550.2:c.894-9001T>A	NP_072044.1:n.894-9001T>A
XM_005248595.1:c.894-8995T>A	XP_005248652.1:n.894-8995T>A
XM_011543626.1:c.894-8995T>A	XP_011541928.1:n.894-8995T>A
XM_011543629.1:c.234-8995T>A	XP_011541931.1:n.234-8995T>A
NM_001318012.1:c.894-8995T>A	NP_001304941.1:n.894-8995T>A
NM_003401.4:c.894-9001T>A	NP_003392.1:n.894-9001T>A
NM_022406.3:c.894-8995T>A	NP_071801.1:n.894-8995T>A
NM_022550.3:c.894-9001T>A	NP_072044.1:n.894-9001T>A
XM_017009827.2:c.894-26137T>A	XP_016865316.1:n.894-26137T>A
NM_001318012.2:c.894-8995T>A	NP_001304941.1:n.894-8995T>A
NM_003401.5:c.894-9001T>A MANE Select	NP_003392.1:n.894-9001T>A
NM_022406.4:c.894-8995T>A	NP_071801.1:n.894-8995T>A
NM_001318012.3:c.894-8995T>A	NP_001304941.1:n.894-8995T>A
NM_022406.5:c.894-8995T>A	NP_071801.1:n.894-8995T>A
NM_022550.4:c.894-9001T>A	NP_072044.1:n.894-9001T>A