Canonical Allele Identifier: CA406363097

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45855823A>T (hg19) ; chr19:g.45352565A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352565A>T , CM000681.2:g.45352565A>T	GRCh38
NC_000019.9:g.45855823A>T , CM000681.1:g.45855823A>T	GRCh37
NC_000019.8:g.50547663A>T	NCBI36
NG_007067.2:g.23023T>A , LRG_461:g.23023T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1987T>A	ENSP00000375808.4:p.Cys663Ser
ENST00000682414.1:c.1987T>A	ENSP00000507019.1:p.Cys663Ser
ENST00000682508.1:n.2016T>A
ENST00000684218.1:c.*1245T>A	ENSP00000507804.1:n.*1245T>A
ENST00000684264.1:n.1543T>A
ENST00000684407.1:c.1864T>A	ENSP00000507775.1:p.Cys622Ser
ENST00000684458.1:c.*473T>A	ENSP00000508260.1:n.*473T>A
ENST00000684468.1:n.1699T>A
ENST00000391945.10:c.1987T>A MANE Select	ENSP00000375809.4:p.Cys663Ser
ENST00000646507.1:n.2084T>A
ENST00000391941.6:c.1915T>A	ENSP00000375805.2:p.Cys639Ser
ENST00000391942.6:n.1158T>A
ENST00000391944.7:c.1753T>A	ENSP00000375808.3:p.Cys585Ser
ENST00000391945.8:c.1987T>A	ENSP00000375809.3:p.Cys663Ser
ENST00000588652.5:n.2075T>A
NM_000400.3:c.1987T>A , LRG_461t1:c.1987T>A	NP_000391.1:p.Cys663Ser
XM_011526611.1:c.1909T>A	XP_011524913.1:p.Cys637Ser
XM_011526611.2:c.1909T>A	XP_011524913.1:p.Cys637Ser
XM_017026467.1:c.1864T>A	XP_016881956.1:p.Cys622Ser
XR_001753633.2:n.2034T>A
XR_001753634.2:n.1970T>A
NM_000400.4:c.1987T>A MANE Select	NP_000391.1:p.Cys663Ser