Canonical Allele Identifier: CA406373280

Gene: ERCC2

Linked Data

• gnomAD v4: 19-45363994-A-T
• MyVariant Identifiers: chr19:g.45867252A>T (hg19) ; chr19:g.45363994A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45363994A>T , CM000681.2:g.45363994A>T	GRCh38
NC_000019.9:g.45867252A>T , CM000681.1:g.45867252A>T	GRCh37
NC_000019.8:g.50559092A>T	NCBI36
NG_007067.2:g.11594T>A , LRG_461:g.11594T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.941T>A	ENSP00000375808.4:p.Val314Glu
ENST00000682414.1:c.941T>A	ENSP00000507019.1:p.Val314Glu
ENST00000682508.1:n.970T>A
ENST00000684218.1:c.*199T>A	ENSP00000507804.1:n.*199T>A
ENST00000684407.1:c.818T>A	ENSP00000507775.1:p.Val273Glu
ENST00000684458.1:c.941T>A	ENSP00000508260.1:p.Val314Glu
ENST00000391945.10:c.941T>A MANE Select	ENSP00000375809.4:p.Val314Glu
ENST00000586131.6:c.869T>A	ENSP00000464887.1:p.Val290Glu
ENST00000587376.6:c.64T>A
ENST00000646507.1:n.1038T>A
ENST00000391941.6:c.869T>A	ENSP00000375805.2:p.Val290Glu
ENST00000391944.7:c.707T>A	ENSP00000375808.3:p.Val236Glu
ENST00000391945.8:c.941T>A	ENSP00000375809.3:p.Val314Glu
ENST00000485403.6:c.869T>A	ENSP00000431229.2:p.Val290Glu
ENST00000586131.5:c.869T>A	ENSP00000464887.1:p.Val290Glu
ENST00000587376.5:c.64T>A
NM_000400.3:c.941T>A , LRG_461t1:c.941T>A	NP_000391.1:p.Val314Glu
NM_001130867.1:c.869T>A	NP_001124339.1:p.Val290Glu
XM_011526611.1:c.863T>A	XP_011524913.1:p.Val288Glu
XR_935763.1:n.988T>A
XM_011526611.2:c.863T>A	XP_011524913.1:p.Val288Glu
XM_017026467.1:c.818T>A	XP_016881956.1:p.Val273Glu
XR_001753633.2:n.988T>A
XR_001753634.2:n.988T>A
NM_000400.4:c.941T>A MANE Select	NP_000391.1:p.Val314Glu
NM_001130867.2:c.869T>A	NP_001124339.1:p.Val290Glu