Canonical Allele Identifier: CA507953549

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45867308G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45364050G>A , CM000681.2:g.45364050G>A	GRCh38
NC_000019.9:g.45867308G>A , CM000681.1:g.45867308G>A	GRCh37
NC_000019.8:g.50559148G>A	NCBI36
NG_007067.2:g.11538C>T , LRG_461:g.11538C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.885C>T	ENSP00000375808.4:p.Ala295=
ENST00000682414.1:c.885C>T	ENSP00000507019.1:p.Ala295=
ENST00000682508.1:n.914C>T
ENST00000684218.1:c.*143C>T	ENSP00000507804.1:n.*143C>T
ENST00000684407.1:c.762C>T	ENSP00000507775.1:p.Ala254=
ENST00000684458.1:c.885C>T	ENSP00000508260.1:p.Ala295=
ENST00000391945.10:c.885C>T MANE Select	ENSP00000375809.4:p.Ala295=
ENST00000586131.6:c.813C>T	ENSP00000464887.1:p.Ala271=
ENST00000587376.6:c.8C>T
ENST00000646507.1:n.982C>T
ENST00000391941.6:c.813C>T	ENSP00000375805.2:p.Ala271=
ENST00000391944.7:c.651C>T	ENSP00000375808.3:p.Ala217=
ENST00000391945.8:c.885C>T	ENSP00000375809.3:p.Ala295=
ENST00000485403.6:c.813C>T	ENSP00000431229.2:p.Ala271=
ENST00000586131.5:c.813C>T	ENSP00000464887.1:p.Ala271=
ENST00000587376.5:c.8C>T
ENST00000591309.5:c.*143C>T	ENSP00000465207.1:n.*143C>T
NM_000400.3:c.885C>T , LRG_461t1:c.885C>T	NP_000391.1:p.Ala295=
NM_001130867.1:c.813C>T	NP_001124339.1:p.Ala271=
XM_011526611.1:c.807C>T	XP_011524913.1:p.Ala269=
XR_935763.1:n.932C>T
XM_011526611.2:c.807C>T	XP_011524913.1:p.Ala269=
XM_017026467.1:c.762C>T	XP_016881956.1:p.Ala254=
XR_001753633.2:n.932C>T
XR_001753634.2:n.932C>T
NM_000400.4:c.885C>T MANE Select	NP_000391.1:p.Ala295=
NM_001130867.2:c.813C>T	NP_001124339.1:p.Ala271=