Canonical Allele Identifier: CA406363528

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45855885T>C (hg19) ; chr19:g.45352627T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352627T>C , CM000681.2:g.45352627T>C	GRCh38
NC_000019.9:g.45855885T>C , CM000681.1:g.45855885T>C	GRCh37
NC_000019.8:g.50547725T>C	NCBI36
NG_007067.2:g.22961A>G , LRG_461:g.22961A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1925A>G	ENSP00000375808.4:p.Asp642Gly
ENST00000682414.1:c.1925A>G	ENSP00000507019.1:p.Asp642Gly
ENST00000682508.1:n.1954A>G
ENST00000684218.1:c.*1183A>G	ENSP00000507804.1:n.*1183A>G
ENST00000684264.1:n.1481A>G
ENST00000684407.1:c.1802A>G	ENSP00000507775.1:p.Asp601Gly
ENST00000684458.1:c.*411A>G	ENSP00000508260.1:n.*411A>G
ENST00000684468.1:n.1637A>G
ENST00000391945.10:c.1925A>G MANE Select	ENSP00000375809.4:p.Asp642Gly
ENST00000646507.1:n.2022A>G
ENST00000391941.6:c.1853A>G	ENSP00000375805.2:p.Asp618Gly
ENST00000391942.6:n.1096A>G
ENST00000391944.7:c.1691A>G	ENSP00000375808.3:p.Asp564Gly
ENST00000391945.8:c.1925A>G	ENSP00000375809.3:p.Asp642Gly
ENST00000588652.5:n.2013A>G
NM_000400.3:c.1925A>G , LRG_461t1:c.1925A>G	NP_000391.1:p.Asp642Gly
XM_011526611.1:c.1847A>G	XP_011524913.1:p.Asp616Gly
XM_011526611.2:c.1847A>G	XP_011524913.1:p.Asp616Gly
XM_017026467.1:c.1802A>G	XP_016881956.1:p.Asp601Gly
XR_001753633.2:n.1972A>G
XR_001753634.2:n.1908A>G
NM_000400.4:c.1925A>G MANE Select	NP_000391.1:p.Asp642Gly