Canonical Allele Identifier: CA406363353
Gene: ERCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45352602G>T , CM000681.2:g.45352602G>T GRCh38
NC_000019.9:g.45855860G>T , CM000681.1:g.45855860G>T GRCh37
NC_000019.8:g.50547700G>T NCBI36
NG_007067.2:g.22986C>A , LRG_461:g.22986C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000391944.8:c.1950C>A ENSP00000375808.4:p.Asp650Glu
ENST00000682414.1:c.1950C>A ENSP00000507019.1:p.Asp650Glu
ENST00000682508.1:n.1979C>A
ENST00000684218.1:c.*1208C>A ENSP00000507804.1:n.*1208C>A
ENST00000684264.1:n.1506C>A
ENST00000684407.1:c.1827C>A ENSP00000507775.1:p.Asp609Glu
ENST00000684458.1:c.*436C>A ENSP00000508260.1:n.*436C>A
ENST00000684468.1:n.1662C>A
ENST00000391945.10:c.1950C>A MANE Select ENSP00000375809.4:p.Asp650Glu
ENST00000646507.1:n.2047C>A
ENST00000391941.6:c.1878C>A ENSP00000375805.2:p.Asp626Glu
ENST00000391942.6:n.1121C>A
ENST00000391944.7:c.1716C>A ENSP00000375808.3:p.Asp572Glu
ENST00000391945.8:c.1950C>A ENSP00000375809.3:p.Asp650Glu
ENST00000588652.5:n.2038C>A
NM_000400.3:c.1950C>A , LRG_461t1:c.1950C>A NP_000391.1:p.Asp650Glu
XM_011526611.1:c.1872C>A XP_011524913.1:p.Asp624Glu
XM_011526611.2:c.1872C>A XP_011524913.1:p.Asp624Glu
XM_017026467.1:c.1827C>A XP_016881956.1:p.Asp609Glu
XR_001753633.2:n.1997C>A
XR_001753634.2:n.1933C>A
NM_000400.4:c.1950C>A MANE Select NP_000391.1:p.Asp650Glu