Canonical Allele Identifier: CA406363017

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45855810G>T (hg19) ; chr19:g.45352552G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352552G>T , CM000681.2:g.45352552G>T	GRCh38
NC_000019.9:g.45855810G>T , CM000681.1:g.45855810G>T	GRCh37
NC_000019.8:g.50547650G>T	NCBI36
NG_007067.2:g.23036C>A , LRG_461:g.23036C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.2000C>A	ENSP00000375808.4:p.Ala667Asp
ENST00000682414.1:c.2000C>A	ENSP00000507019.1:p.Ala667Asp
ENST00000682508.1:n.2029C>A
ENST00000684218.1:c.*1258C>A	ENSP00000507804.1:n.*1258C>A
ENST00000684264.1:n.1556C>A
ENST00000684407.1:c.1877C>A	ENSP00000507775.1:p.Ala626Asp
ENST00000684458.1:c.*486C>A	ENSP00000508260.1:n.*486C>A
ENST00000684468.1:n.1712C>A
ENST00000391945.10:c.2000C>A MANE Select	ENSP00000375809.4:p.Ala667Asp
ENST00000646507.1:n.2097C>A
ENST00000391941.6:c.1928C>A	ENSP00000375805.2:p.Ala643Asp
ENST00000391942.6:n.1171C>A
ENST00000391944.7:c.1766C>A	ENSP00000375808.3:p.Ala589Asp
ENST00000391945.8:c.2000C>A	ENSP00000375809.3:p.Ala667Asp
ENST00000588652.5:n.2088C>A
NM_000400.3:c.2000C>A , LRG_461t1:c.2000C>A	NP_000391.1:p.Ala667Asp
XM_011526611.1:c.1922C>A	XP_011524913.1:p.Ala641Asp
XM_011526611.2:c.1922C>A	XP_011524913.1:p.Ala641Asp
XM_017026467.1:c.1877C>A	XP_016881956.1:p.Ala626Asp
XR_001753633.2:n.2047C>A
XR_001753634.2:n.1983C>A
NM_000400.4:c.2000C>A MANE Select	NP_000391.1:p.Ala667Asp