Canonical Allele Identifier: CA406373620

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45867323C>G (hg19) ; chr19:g.45364065C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45364065C>G , CM000681.2:g.45364065C>G	GRCh38
NC_000019.9:g.45867323C>G , CM000681.1:g.45867323C>G	GRCh37
NC_000019.8:g.50559163C>G	NCBI36
NG_007067.2:g.11523G>C , LRG_461:g.11523G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.870G>C	ENSP00000375808.4:p.Glu290Asp
ENST00000682414.1:c.870G>C	ENSP00000507019.1:p.Glu290Asp
ENST00000682508.1:n.899G>C
ENST00000684218.1:c.*128G>C	ENSP00000507804.1:n.*128G>C
ENST00000684407.1:c.747G>C	ENSP00000507775.1:p.Glu249Asp
ENST00000684458.1:c.870G>C	ENSP00000508260.1:p.Glu290Asp
ENST00000391945.10:c.870G>C MANE Select	ENSP00000375809.4:p.Glu290Asp
ENST00000586131.6:c.798G>C	ENSP00000464887.1:p.Glu266Asp
ENST00000646507.1:n.967G>C
ENST00000391941.6:c.798G>C	ENSP00000375805.2:p.Glu266Asp
ENST00000391944.7:c.636G>C	ENSP00000375808.3:p.Glu212Asp
ENST00000391945.8:c.870G>C	ENSP00000375809.3:p.Glu290Asp
ENST00000485403.6:c.798G>C	ENSP00000431229.2:p.Glu266Asp
ENST00000586131.5:c.798G>C	ENSP00000464887.1:p.Glu266Asp
ENST00000591309.5:c.*128G>C	ENSP00000465207.1:n.*128G>C
NM_000400.3:c.870G>C , LRG_461t1:c.870G>C	NP_000391.1:p.Glu290Asp
NM_001130867.1:c.798G>C	NP_001124339.1:p.Glu266Asp
XM_011526611.1:c.792G>C	XP_011524913.1:p.Glu264Asp
XR_935763.1:n.917G>C
XM_011526611.2:c.792G>C	XP_011524913.1:p.Glu264Asp
XM_017026467.1:c.747G>C	XP_016881956.1:p.Glu249Asp
XR_001753633.2:n.917G>C
XR_001753634.2:n.917G>C
NM_000400.4:c.870G>C MANE Select	NP_000391.1:p.Glu290Asp
NM_001130867.2:c.798G>C	NP_001124339.1:p.Glu266Asp