Canonical Allele Identifier: CA996296171
Gene: ERCC2 HGNC NCBI

Linked Data

dbSNP Id: rs1971906675

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45353605_45353610dup , CM000681.2:g.45353605_45353610dup GRCh38
NC_000019.9:g.45856863_45856868dup , CM000681.1:g.45856863_45856868dup GRCh37
NC_000019.8:g.50548703_50548708dup NCBI36
NG_007067.2:g.21979_21984dup , LRG_461:g.21979_21984dup

Transcript Alleles

HGVS Amino-acid change
ENST00000391944.8:c.1666-275_1666-270dup ENSP00000375808.4:n.1666-275_1666-270dup
ENST00000682414.1:c.1666-275_1666-270dup ENSP00000507019.1:n.1666-275_1666-270dup
ENST00000682508.1:n.1695-275_1695-270dup
ENST00000684218.1:c.*924-275_*924-270dup ENSP00000507804.1:n.*924-275_*924-270dup
ENST00000684264.1:n.1222-275_1222-270dup
ENST00000684407.1:c.1543-275_1543-270dup ENSP00000507775.1:n.1543-275_1543-270dup
ENST00000684458.1:c.*152-275_*152-270dup ENSP00000508260.1:n.*152-275_*152-270dup
ENST00000684468.1:n.1378-275_1378-270dup
ENST00000391945.10:c.1666-275_1666-270dup MANE Select ENSP00000375809.4:n.1666-275_1666-270dup
ENST00000587376.6:c.725-275_725-270dup
ENST00000646507.1:n.1763-275_1763-270dup
ENST00000391941.6:c.1594-275_1594-270dup ENSP00000375805.2:n.1594-275_1594-270dup
ENST00000391942.6:n.837-275_837-270dup
ENST00000391944.7:c.1432-275_1432-270dup ENSP00000375808.3:n.1432-275_1432-270dup
ENST00000391945.8:c.1666-275_1666-270dup ENSP00000375809.3:n.1666-275_1666-270dup
ENST00000587376.5:c.725-275_725-270dup
ENST00000588652.5:n.1754-275_1754-270dup
NM_000400.3:c.1666-275_1666-270dup , LRG_461t1:c.1666-275_1666-270dup NP_000391.1:n.1666-275_1666-270dup
XM_011526611.1:c.1588-275_1588-270dup XP_011524913.1:n.1588-275_1588-270dup
XR_935763.1:n.1649-275_1649-270dup
XM_011526611.2:c.1588-275_1588-270dup XP_011524913.1:n.1588-275_1588-270dup
XM_017026467.1:c.1543-275_1543-270dup XP_016881956.1:n.1543-275_1543-270dup
XR_001753633.2:n.1713-275_1713-270dup
XR_001753634.2:n.1649-275_1649-270dup
NM_000400.4:c.1666-275_1666-270dup MANE Select NP_000391.1:n.1666-275_1666-270dup