Canonical Allele Identifier: CA406362669

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45855765T>A (hg19) ; chr19:g.45352507T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352507T>A , CM000681.2:g.45352507T>A	GRCh38
NC_000019.9:g.45855765T>A , CM000681.1:g.45855765T>A	GRCh37
NC_000019.8:g.50547605T>A	NCBI36
NG_007067.2:g.23081A>T , LRG_461:g.23081A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000391944.8:c.2045A>T	ENSP00000375808.4:p.Lys682Met
ENST00000682414.1:c.2045A>T	ENSP00000507019.1:p.Lys682Met
ENST00000682508.1:n.2074A>T
ENST00000684218.1:c.*1303A>T	ENSP00000507804.1:n.*1303A>T
ENST00000684264.1:n.1601A>T
ENST00000684407.1:c.1922A>T	ENSP00000507775.1:p.Lys641Met
ENST00000684458.1:c.*531A>T	ENSP00000508260.1:n.*531A>T
ENST00000684468.1:n.1757A>T
ENST00000391945.10:c.2045A>T MANE Select	ENSP00000375809.4:p.Lys682Met
ENST00000646507.1:n.2142A>T
ENST00000391941.6:c.1973A>T	ENSP00000375805.2:p.Lys658Met
ENST00000391942.6:n.1216A>T
ENST00000391944.7:c.1811A>T	ENSP00000375808.3:p.Lys604Met
ENST00000391945.8:c.2045A>T	ENSP00000375809.3:p.Lys682Met
ENST00000588652.5:n.2133A>T
NM_000400.3:c.2045A>T , LRG_461t1:c.2045A>T	NP_000391.1:p.Lys682Met
XM_011526611.1:c.1967A>T	XP_011524913.1:p.Lys656Met
XM_011526611.2:c.1967A>T	XP_011524913.1:p.Lys656Met
XM_017026467.1:c.1922A>T	XP_016881956.1:p.Lys641Met
XR_001753633.2:n.2092A>T
XR_001753634.2:n.2028A>T
NM_000400.4:c.2045A>T MANE Select	NP_000391.1:p.Lys682Met