Canonical Allele Identifier: CA9512959
Gene: ERCC2 HGNC NCBI

Linked Data

dbSNP Id: rs762985501

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45352590G>T , CM000681.2:g.45352590G>T GRCh38
NC_000019.9:g.45855848G>T , CM000681.1:g.45855848G>T GRCh37
NC_000019.8:g.50547688G>T NCBI36
NG_007067.2:g.22998C>A , LRG_461:g.22998C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000391944.8:c.1962C>A ENSP00000375808.4:p.Phe654Leu
ENST00000682414.1:c.1962C>A ENSP00000507019.1:p.Phe654Leu
ENST00000682508.1:n.1991C>A
ENST00000684218.1:c.*1220C>A ENSP00000507804.1:n.*1220C>A
ENST00000684264.1:n.1518C>A
ENST00000684407.1:c.1839C>A ENSP00000507775.1:p.Phe613Leu
ENST00000684458.1:c.*448C>A ENSP00000508260.1:n.*448C>A
ENST00000684468.1:n.1674C>A
ENST00000391945.10:c.1962C>A MANE Select ENSP00000375809.4:p.Phe654Leu
ENST00000646507.1:n.2059C>A
ENST00000391941.6:c.1890C>A ENSP00000375805.2:p.Phe630Leu
ENST00000391942.6:n.1133C>A
ENST00000391944.7:c.1728C>A ENSP00000375808.3:p.Phe576Leu
ENST00000391945.8:c.1962C>A ENSP00000375809.3:p.Phe654Leu
ENST00000588652.5:n.2050C>A
NM_000400.3:c.1962C>A , LRG_461t1:c.1962C>A NP_000391.1:p.Phe654Leu
XM_011526611.1:c.1884C>A XP_011524913.1:p.Phe628Leu
XM_011526611.2:c.1884C>A XP_011524913.1:p.Phe628Leu
XM_017026467.1:c.1839C>A XP_016881956.1:p.Phe613Leu
XR_001753633.2:n.2009C>A
XR_001753634.2:n.1945C>A
NM_000400.4:c.1962C>A MANE Select NP_000391.1:p.Phe654Leu