Canonical Allele Identifier: CA406363748

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45856023G>C (hg19) ; chr19:g.45352765G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352765G>C , CM000681.2:g.45352765G>C	GRCh38
NC_000019.9:g.45856023G>C , CM000681.1:g.45856023G>C	GRCh37
NC_000019.8:g.50547863G>C	NCBI36
NG_007067.2:g.22823C>G , LRG_461:g.22823C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1883C>G	ENSP00000375808.4:p.Thr628Arg
ENST00000682414.1:c.1883C>G	ENSP00000507019.1:p.Thr628Arg
ENST00000682508.1:n.1912C>G
ENST00000684218.1:c.*1141C>G	ENSP00000507804.1:n.*1141C>G
ENST00000684264.1:n.1439C>G
ENST00000684407.1:c.1760C>G	ENSP00000507775.1:p.Thr587Arg
ENST00000684458.1:c.*369C>G	ENSP00000508260.1:n.*369C>G
ENST00000684468.1:n.1595C>G
ENST00000391945.10:c.1883C>G MANE Select	ENSP00000375809.4:p.Thr628Arg
ENST00000646507.1:n.1980C>G
ENST00000391941.6:c.1811C>G	ENSP00000375805.2:p.Thr604Arg
ENST00000391942.6:n.1054C>G
ENST00000391944.7:c.1649C>G	ENSP00000375808.3:p.Thr550Arg
ENST00000391945.8:c.1883C>G	ENSP00000375809.3:p.Thr628Arg
ENST00000588652.5:n.1971C>G
NM_000400.3:c.1883C>G , LRG_461t1:c.1883C>G	NP_000391.1:p.Thr628Arg
XM_011526611.1:c.1805C>G	XP_011524913.1:p.Thr602Arg
XM_011526611.2:c.1805C>G	XP_011524913.1:p.Thr602Arg
XM_017026467.1:c.1760C>G	XP_016881956.1:p.Thr587Arg
XR_001753633.2:n.1930C>G
XR_001753634.2:n.1866C>G
NM_000400.4:c.1883C>G MANE Select	NP_000391.1:p.Thr628Arg