Canonical Allele Identifier: CA406362323

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45855563C>G (hg19) ; chr19:g.45352305C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352305C>G , CM000681.2:g.45352305C>G	GRCh38
NC_000019.9:g.45855563C>G , CM000681.1:g.45855563C>G	GRCh37
NC_000019.8:g.50547403C>G	NCBI36
NG_007067.2:g.23283G>C , LRG_461:g.23283G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.2094G>C	ENSP00000375808.4:p.Gln698His
ENST00000682414.1:c.2094G>C	ENSP00000507019.1:p.Gln698His
ENST00000682508.1:n.2123G>C
ENST00000684218.1:c.*1352G>C	ENSP00000507804.1:n.*1352G>C
ENST00000684264.1:n.1650G>C
ENST00000684407.1:c.1971G>C	ENSP00000507775.1:p.Gln657His
ENST00000684458.1:c.*580G>C	ENSP00000508260.1:n.*580G>C
ENST00000684468.1:n.1806G>C
ENST00000391945.10:c.2094G>C MANE Select	ENSP00000375809.4:p.Gln698His
ENST00000646507.1:n.2191G>C
ENST00000391941.6:c.2022G>C	ENSP00000375805.2:p.Gln674His
ENST00000391942.6:n.1265G>C
ENST00000391944.7:c.1860G>C	ENSP00000375808.3:p.Gln620His
ENST00000391945.8:c.2094G>C	ENSP00000375809.3:p.Gln698His
ENST00000588652.5:n.2182G>C
NM_000400.3:c.2094G>C , LRG_461t1:c.2094G>C	NP_000391.1:p.Gln698His
XM_011526611.1:c.2016G>C	XP_011524913.1:p.Gln672His
XM_011526611.2:c.2016G>C	XP_011524913.1:p.Gln672His
XM_017026467.1:c.1971G>C	XP_016881956.1:p.Gln657His
XR_001753633.2:n.2141G>C
XR_001753634.2:n.2077G>C
NM_000400.4:c.2094G>C MANE Select	NP_000391.1:p.Gln698His