Canonical Allele Identifier: CA406362174

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45855535G>T (hg19) ; chr19:g.45352277G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352277G>T , CM000681.2:g.45352277G>T	GRCh38
NC_000019.9:g.45855535G>T , CM000681.1:g.45855535G>T	GRCh37
NC_000019.8:g.50547375G>T	NCBI36
NG_007067.2:g.23311C>A , LRG_461:g.23311C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.2122C>A	ENSP00000375808.4:p.Leu708Met
ENST00000682414.1:c.2122C>A	ENSP00000507019.1:p.Leu708Met
ENST00000682508.1:n.2151C>A
ENST00000684218.1:c.*1380C>A	ENSP00000507804.1:n.*1380C>A
ENST00000684264.1:n.1678C>A
ENST00000684407.1:c.1999C>A	ENSP00000507775.1:p.Leu667Met
ENST00000684458.1:c.*608C>A	ENSP00000508260.1:n.*608C>A
ENST00000684468.1:n.1834C>A
ENST00000391945.10:c.2122C>A MANE Select	ENSP00000375809.4:p.Leu708Met
ENST00000646507.1:n.2219C>A
ENST00000391941.6:c.2050C>A	ENSP00000375805.2:p.Leu684Met
ENST00000391942.6:n.1293C>A
ENST00000391944.7:c.1888C>A	ENSP00000375808.3:p.Leu630Met
ENST00000391945.8:c.2122C>A	ENSP00000375809.3:p.Leu708Met
ENST00000588652.5:n.2210C>A
NM_000400.3:c.2122C>A , LRG_461t1:c.2122C>A	NP_000391.1:p.Leu708Met
XM_011526611.1:c.2044C>A	XP_011524913.1:p.Leu682Met
XM_011526611.2:c.2044C>A	XP_011524913.1:p.Leu682Met
XM_017026467.1:c.1999C>A	XP_016881956.1:p.Leu667Met
XR_001753633.2:n.2169C>A
XR_001753634.2:n.2105C>A
NM_000400.4:c.2122C>A MANE Select	NP_000391.1:p.Leu708Met