Canonical Allele Identifier: CA2338389365

Gene: ERCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45353240_45353245delinsACCTCC , CM000681.2:g.45353240_45353245delinsACCTCC	GRCh38
NC_000019.9:g.45856498_45856503delinsACCTCC , CM000681.1:g.45856498_45856503delinsACCTCC	GRCh37
NC_000019.8:g.50548338_50548343delinsACCTCC	NCBI36
NG_007067.2:g.22343_22348delinsGGAGGT , LRG_461:g.22343_22348delinsGGAGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1755_1758+2delinsGGAGGT
ENST00000682414.1:c.1755_1758+2delinsGGAGGT
ENST00000682508.1:n.1784_1787+2delinsGGAGGT
ENST00000684218.1:c.*1013_*1016+2delinsGGAGGT
ENST00000684264.1:n.1311_1314+2delinsGGAGGT
ENST00000684407.1:c.1632_1635+2delinsGGAGGT
ENST00000684458.1:c.*241_*244+2delinsGGAGGT
ENST00000684468.1:n.1467_1470+2delinsGGAGGT
ENST00000391945.10:c.1755_1758+2delinsGGAGGT
ENST00000587376.6:c.814_817+2delinsGGAGGT
ENST00000646507.1:n.1852_1855+2delinsGGAGGT
ENST00000391941.6:c.1683_1686+2delinsGGAGGT
ENST00000391942.6:n.926_929+2delinsGGAGGT
ENST00000391944.7:c.1521_1524+2delinsGGAGGT
ENST00000391945.8:c.1755_1758+2delinsGGAGGT
ENST00000588652.5:n.1843_1846+2delinsGGAGGT
NM_000400.3:c.1755_1758+2delinsGGAGGT , LRG_461t1:c.1755_1758+2delinsGGAGGT
XM_011526611.1:c.1677_1680+2delinsGGAGGT
XM_011526611.2:c.1677_1680+2delinsGGAGGT
XM_017026467.1:c.1632_1635+2delinsGGAGGT
XR_001753633.2:n.1802_1805+2delinsGGAGGT
XR_001753634.2:n.1738_1741+2delinsGGAGGT
NM_000400.4:c.1755_1758+2delinsGGAGGT