Canonical Allele Identifier: CA1329085303

Gene: NHEJ1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219158123_219158128delinsACAGGC , CM000664.2:g.219158123_219158128delinsACAGGC	GRCh38
NC_000002.11:g.220022845_220022850delinsACAGGC , CM000664.1:g.220022845_220022850delinsACAGGC	GRCh37
NC_000002.10:g.219731089_219731094delinsACAGGC	NCBI36
NG_007880.1:g.7738_7743delinsGCCTGT , LRG_90:g.7738_7743delinsGCCTGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000426304.6:c.177+58_177+63delinsGCCTGT	ENSP00000394896.2:n.177+58_177+63delinsGCCTGT
ENST00000457600.3:c.177+58_177+63delinsGCCTGT	ENSP00000407201.2:n.177+58_177+63delinsGCCTGT
ENST00000698174.1:c.177+58_177+63delinsGCCTGT	ENSP00000513594.1:n.177+58_177+63delinsGCCTGT
ENST00000698175.1:c.177+58_177+63delinsGCCTGT	ENSP00000513595.1:n.177+58_177+63delinsGCCTGT
ENST00000698176.1:n.249+58_249+63delinsGCCTGT
ENST00000698202.1:c.177+58_177+63delinsGCCTGT	ENSP00000513605.1:n.177+58_177+63delinsGCCTGT
ENST00000698203.1:c.177+58_177+63delinsGCCTGT	ENSP00000513606.1:n.177+58_177+63delinsGCCTGT
ENST00000356853.10:c.177+58_177+63delinsGCCTGT MANE Select	ENSP00000349313.5:n.177+58_177+63delinsGCCTGT
ENST00000318673.6:c.*1299+58_*1299+63delinsGCCTGT	ENSP00000320919.3:n.*1299+58_*1299+63delinsGCCTGT
ENST00000356853.9:c.177+58_177+63delinsGCCTGT	ENSP00000349313.5:n.177+58_177+63delinsGCCTGT
ENST00000409720.5:c.177+58_177+63delinsGCCTGT	ENSP00000387290.1:n.177+58_177+63delinsGCCTGT
ENST00000418099.5:c.177+58_177+63delinsGCCTGT	ENSP00000408966.1:n.177+58_177+63delinsGCCTGT
ENST00000450447.1:c.144+91_144+96delinsGCCTGT	ENSP00000408421.1:n.144+91_144+96delinsGCCTGT
ENST00000457600.2:c.177+58_177+63delinsGCCTGT	ENSP00000407201.1:n.177+58_177+63delinsGCCTGT
ENST00000498327.5:n.2365+58_2365+63delinsGCCTGT
NM_024782.2:c.177+58_177+63delinsGCCTGT , LRG_90t1:c.177+58_177+63delinsGCCTGT	NP_079058.1:n.177+58_177+63delinsGCCTGT
NM_001377498.1:c.177+58_177+63delinsGCCTGT	NP_001364427.1:n.177+58_177+63delinsGCCTGT
NM_001377499.1:c.177+58_177+63delinsGCCTGT	NP_001364428.1:n.177+58_177+63delinsGCCTGT
NM_024782.3:c.177+58_177+63delinsGCCTGT MANE Select	NP_079058.1:n.177+58_177+63delinsGCCTGT
NR_165304.1:n.273+58_273+63delinsGCCTGT