Canonical Allele Identifier: CA406362682

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45855766T>A (hg19) ; chr19:g.45352508T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352508T>A , CM000681.2:g.45352508T>A	GRCh38
NC_000019.9:g.45855766T>A , CM000681.1:g.45855766T>A	GRCh37
NC_000019.8:g.50547606T>A	NCBI36
NG_007067.2:g.23080A>T , LRG_461:g.23080A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000391944.8:c.2044A>T	ENSP00000375808.4:p.Lys682Ter
ENST00000682414.1:c.2044A>T	ENSP00000507019.1:p.Lys682Ter
ENST00000682508.1:n.2073A>T
ENST00000684218.1:c.*1302A>T	ENSP00000507804.1:n.*1302A>T
ENST00000684264.1:n.1600A>T
ENST00000684407.1:c.1921A>T	ENSP00000507775.1:p.Lys641Ter
ENST00000684458.1:c.*530A>T	ENSP00000508260.1:n.*530A>T
ENST00000684468.1:n.1756A>T
ENST00000391945.10:c.2044A>T MANE Select	ENSP00000375809.4:p.Lys682Ter
ENST00000646507.1:n.2141A>T
ENST00000391941.6:c.1972A>T	ENSP00000375805.2:p.Lys658Ter
ENST00000391942.6:n.1215A>T
ENST00000391944.7:c.1810A>T	ENSP00000375808.3:p.Lys604Ter
ENST00000391945.8:c.2044A>T	ENSP00000375809.3:p.Lys682Ter
ENST00000588652.5:n.2132A>T
NM_000400.3:c.2044A>T , LRG_461t1:c.2044A>T	NP_000391.1:p.Lys682Ter
XM_011526611.1:c.1966A>T	XP_011524913.1:p.Lys656Ter
XM_011526611.2:c.1966A>T	XP_011524913.1:p.Lys656Ter
XM_017026467.1:c.1921A>T	XP_016881956.1:p.Lys641Ter
XR_001753633.2:n.2091A>T
XR_001753634.2:n.2027A>T
NM_000400.4:c.2044A>T MANE Select	NP_000391.1:p.Lys682Ter