Canonical Allele Identifier: CA406362514

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45855601G>C (hg19) ; chr19:g.45352343G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352343G>C , CM000681.2:g.45352343G>C	GRCh38
NC_000019.9:g.45855601G>C , CM000681.1:g.45855601G>C	GRCh37
NC_000019.8:g.50547441G>C	NCBI36
NG_007067.2:g.23245C>G , LRG_461:g.23245C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000391944.8:c.2056C>G	ENSP00000375808.4:p.Arg686Gly
ENST00000682414.1:c.2056C>G	ENSP00000507019.1:p.Arg686Gly
ENST00000682508.1:n.2085C>G
ENST00000684218.1:c.*1314C>G	ENSP00000507804.1:n.*1314C>G
ENST00000684264.1:n.1612C>G
ENST00000684407.1:c.1933C>G	ENSP00000507775.1:p.Arg645Gly
ENST00000684458.1:c.*542C>G	ENSP00000508260.1:n.*542C>G
ENST00000684468.1:n.1768C>G
ENST00000391945.10:c.2056C>G MANE Select	ENSP00000375809.4:p.Arg686Gly
ENST00000646507.1:n.2153C>G
ENST00000391941.6:c.1984C>G	ENSP00000375805.2:p.Arg662Gly
ENST00000391942.6:n.1227C>G
ENST00000391944.7:c.1822C>G	ENSP00000375808.3:p.Arg608Gly
ENST00000391945.8:c.2056C>G	ENSP00000375809.3:p.Arg686Gly
ENST00000588652.5:n.2144C>G
NM_000400.3:c.2056C>G , LRG_461t1:c.2056C>G	NP_000391.1:p.Arg686Gly
XM_011526611.1:c.1978C>G	XP_011524913.1:p.Arg660Gly
XM_011526611.2:c.1978C>G	XP_011524913.1:p.Arg660Gly
XM_017026467.1:c.1933C>G	XP_016881956.1:p.Arg645Gly
XR_001753633.2:n.2103C>G
XR_001753634.2:n.2039C>G
NM_000400.4:c.2056C>G MANE Select	NP_000391.1:p.Arg686Gly