Canonical Allele Identifier: CA406363878

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45856053A>T (hg19) ; chr19:g.45352795A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352795A>T , CM000681.2:g.45352795A>T	GRCh38
NC_000019.9:g.45856053A>T , CM000681.1:g.45856053A>T	GRCh37
NC_000019.8:g.50547893A>T	NCBI36
NG_007067.2:g.22793T>A , LRG_461:g.22793T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1853T>A	ENSP00000375808.4:p.Val618Asp
ENST00000682414.1:c.1853T>A	ENSP00000507019.1:p.Val618Asp
ENST00000682508.1:n.1882T>A
ENST00000684218.1:c.*1111T>A	ENSP00000507804.1:n.*1111T>A
ENST00000684264.1:n.1409T>A
ENST00000684407.1:c.1730T>A	ENSP00000507775.1:p.Val577Asp
ENST00000684458.1:c.*339T>A	ENSP00000508260.1:n.*339T>A
ENST00000684468.1:n.1565T>A
ENST00000391945.10:c.1853T>A MANE Select	ENSP00000375809.4:p.Val618Asp
ENST00000646507.1:n.1950T>A
ENST00000391941.6:c.1781T>A	ENSP00000375805.2:p.Val594Asp
ENST00000391942.6:n.1024T>A
ENST00000391944.7:c.1619T>A	ENSP00000375808.3:p.Val540Asp
ENST00000391945.8:c.1853T>A	ENSP00000375809.3:p.Val618Asp
ENST00000588652.5:n.1941T>A
NM_000400.3:c.1853T>A , LRG_461t1:c.1853T>A	NP_000391.1:p.Val618Asp
XM_011526611.1:c.1775T>A	XP_011524913.1:p.Val592Asp
XM_011526611.2:c.1775T>A	XP_011524913.1:p.Val592Asp
XM_017026467.1:c.1730T>A	XP_016881956.1:p.Val577Asp
XR_001753633.2:n.1900T>A
XR_001753634.2:n.1836T>A
NM_000400.4:c.1853T>A MANE Select	NP_000391.1:p.Val618Asp