Canonical Allele Identifier: CA406362999

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45855807A>G (hg19) ; chr19:g.45352549A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352549A>G , CM000681.2:g.45352549A>G	GRCh38
NC_000019.9:g.45855807A>G , CM000681.1:g.45855807A>G	GRCh37
NC_000019.8:g.50547647A>G	NCBI36
NG_007067.2:g.23039T>C , LRG_461:g.23039T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.2003T>C	ENSP00000375808.4:p.Ile668Thr
ENST00000682414.1:c.2003T>C	ENSP00000507019.1:p.Ile668Thr
ENST00000682508.1:n.2032T>C
ENST00000684218.1:c.*1261T>C	ENSP00000507804.1:n.*1261T>C
ENST00000684264.1:n.1559T>C
ENST00000684407.1:c.1880T>C	ENSP00000507775.1:p.Ile627Thr
ENST00000684458.1:c.*489T>C	ENSP00000508260.1:n.*489T>C
ENST00000684468.1:n.1715T>C
ENST00000391945.10:c.2003T>C MANE Select	ENSP00000375809.4:p.Ile668Thr
ENST00000646507.1:n.2100T>C
ENST00000391941.6:c.1931T>C	ENSP00000375805.2:p.Ile644Thr
ENST00000391942.6:n.1174T>C
ENST00000391944.7:c.1769T>C	ENSP00000375808.3:p.Ile590Thr
ENST00000391945.8:c.2003T>C	ENSP00000375809.3:p.Ile668Thr
ENST00000588652.5:n.2091T>C
NM_000400.3:c.2003T>C , LRG_461t1:c.2003T>C	NP_000391.1:p.Ile668Thr
XM_011526611.1:c.1925T>C	XP_011524913.1:p.Ile642Thr
XM_011526611.2:c.1925T>C	XP_011524913.1:p.Ile642Thr
XM_017026467.1:c.1880T>C	XP_016881956.1:p.Ile627Thr
XR_001753633.2:n.2050T>C
XR_001753634.2:n.1986T>C
NM_000400.4:c.2003T>C MANE Select	NP_000391.1:p.Ile668Thr