Canonical Allele Identifier: CA406363188

Gene: ERCC2

Linked Data

• COSMIC: COSM418172
• MyVariant Identifiers: chr19:g.45855835G>A (hg19) ; chr19:g.45352577G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352577G>A , CM000681.2:g.45352577G>A	GRCh38
NC_000019.9:g.45855835G>A , CM000681.1:g.45855835G>A	GRCh37
NC_000019.8:g.50547675G>A	NCBI36
NG_007067.2:g.23011C>T , LRG_461:g.23011C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000391944.8:c.1975C>T	ENSP00000375808.4:p.His659Tyr
ENST00000682414.1:c.1975C>T	ENSP00000507019.1:p.His659Tyr
ENST00000682508.1:n.2004C>T
ENST00000684218.1:c.*1233C>T	ENSP00000507804.1:n.*1233C>T
ENST00000684264.1:n.1531C>T
ENST00000684407.1:c.1852C>T	ENSP00000507775.1:p.His618Tyr
ENST00000684458.1:c.*461C>T	ENSP00000508260.1:n.*461C>T
ENST00000684468.1:n.1687C>T
ENST00000391945.10:c.1975C>T MANE Select	ENSP00000375809.4:p.His659Tyr
ENST00000646507.1:n.2072C>T
ENST00000391941.6:c.1903C>T	ENSP00000375805.2:p.His635Tyr
ENST00000391942.6:n.1146C>T
ENST00000391944.7:c.1741C>T	ENSP00000375808.3:p.His581Tyr
ENST00000391945.8:c.1975C>T	ENSP00000375809.3:p.His659Tyr
ENST00000588652.5:n.2063C>T
NM_000400.3:c.1975C>T , LRG_461t1:c.1975C>T	NP_000391.1:p.His659Tyr
XM_011526611.1:c.1897C>T	XP_011524913.1:p.His633Tyr
XM_011526611.2:c.1897C>T	XP_011524913.1:p.His633Tyr
XM_017026467.1:c.1852C>T	XP_016881956.1:p.His618Tyr
XR_001753633.2:n.2022C>T
XR_001753634.2:n.1958C>T
NM_000400.4:c.1975C>T MANE Select	NP_000391.1:p.His659Tyr