Canonical Allele Identifier: CA406363363
Gene: ERCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45352603T>C , CM000681.2:g.45352603T>C GRCh38
NC_000019.9:g.45855861T>C , CM000681.1:g.45855861T>C GRCh37
NC_000019.8:g.50547701T>C NCBI36
NG_007067.2:g.22985A>G , LRG_461:g.22985A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000391944.8:c.1949A>G ENSP00000375808.4:p.Asp650Gly
ENST00000682414.1:c.1949A>G ENSP00000507019.1:p.Asp650Gly
ENST00000682508.1:n.1978A>G
ENST00000684218.1:c.*1207A>G ENSP00000507804.1:n.*1207A>G
ENST00000684264.1:n.1505A>G
ENST00000684407.1:c.1826A>G ENSP00000507775.1:p.Asp609Gly
ENST00000684458.1:c.*435A>G ENSP00000508260.1:n.*435A>G
ENST00000684468.1:n.1661A>G
ENST00000391945.10:c.1949A>G MANE Select ENSP00000375809.4:p.Asp650Gly
ENST00000646507.1:n.2046A>G
ENST00000391941.6:c.1877A>G ENSP00000375805.2:p.Asp626Gly
ENST00000391942.6:n.1120A>G
ENST00000391944.7:c.1715A>G ENSP00000375808.3:p.Asp572Gly
ENST00000391945.8:c.1949A>G ENSP00000375809.3:p.Asp650Gly
ENST00000588652.5:n.2037A>G
NM_000400.3:c.1949A>G , LRG_461t1:c.1949A>G NP_000391.1:p.Asp650Gly
XM_011526611.1:c.1871A>G XP_011524913.1:p.Asp624Gly
XM_011526611.2:c.1871A>G XP_011524913.1:p.Asp624Gly
XM_017026467.1:c.1826A>G XP_016881956.1:p.Asp609Gly
XR_001753633.2:n.1996A>G
XR_001753634.2:n.1932A>G
NM_000400.4:c.1949A>G MANE Select NP_000391.1:p.Asp650Gly