Canonical Allele Identifier: CA406363311

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45855853T>C (hg19) ; chr19:g.45352595T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352595T>C , CM000681.2:g.45352595T>C	GRCh38
NC_000019.9:g.45855853T>C , CM000681.1:g.45855853T>C	GRCh37
NC_000019.8:g.50547693T>C	NCBI36
NG_007067.2:g.22993A>G , LRG_461:g.22993A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1957A>G	ENSP00000375808.4:p.Thr653Ala
ENST00000682414.1:c.1957A>G	ENSP00000507019.1:p.Thr653Ala
ENST00000682508.1:n.1986A>G
ENST00000684218.1:c.*1215A>G	ENSP00000507804.1:n.*1215A>G
ENST00000684264.1:n.1513A>G
ENST00000684407.1:c.1834A>G	ENSP00000507775.1:p.Thr612Ala
ENST00000684458.1:c.*443A>G	ENSP00000508260.1:n.*443A>G
ENST00000684468.1:n.1669A>G
ENST00000391945.10:c.1957A>G MANE Select	ENSP00000375809.4:p.Thr653Ala
ENST00000646507.1:n.2054A>G
ENST00000391941.6:c.1885A>G	ENSP00000375805.2:p.Thr629Ala
ENST00000391942.6:n.1128A>G
ENST00000391944.7:c.1723A>G	ENSP00000375808.3:p.Thr575Ala
ENST00000391945.8:c.1957A>G	ENSP00000375809.3:p.Thr653Ala
ENST00000588652.5:n.2045A>G
NM_000400.3:c.1957A>G , LRG_461t1:c.1957A>G	NP_000391.1:p.Thr653Ala
XM_011526611.1:c.1879A>G	XP_011524913.1:p.Thr627Ala
XM_011526611.2:c.1879A>G	XP_011524913.1:p.Thr627Ala
XM_017026467.1:c.1834A>G	XP_016881956.1:p.Thr612Ala
XR_001753633.2:n.2004A>G
XR_001753634.2:n.1940A>G
NM_000400.4:c.1957A>G MANE Select	NP_000391.1:p.Thr653Ala