Canonical Allele Identifier: CA406363422

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45855873A>T (hg19) ; chr19:g.45352615A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352615A>T , CM000681.2:g.45352615A>T	GRCh38
NC_000019.9:g.45855873A>T , CM000681.1:g.45855873A>T	GRCh37
NC_000019.8:g.50547713A>T	NCBI36
NG_007067.2:g.22973T>A , LRG_461:g.22973T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1937T>A	ENSP00000375808.4:p.Ile646Asn
ENST00000682414.1:c.1937T>A	ENSP00000507019.1:p.Ile646Asn
ENST00000682508.1:n.1966T>A
ENST00000684218.1:c.*1195T>A	ENSP00000507804.1:n.*1195T>A
ENST00000684264.1:n.1493T>A
ENST00000684407.1:c.1814T>A	ENSP00000507775.1:p.Ile605Asn
ENST00000684458.1:c.*423T>A	ENSP00000508260.1:n.*423T>A
ENST00000684468.1:n.1649T>A
ENST00000391945.10:c.1937T>A MANE Select	ENSP00000375809.4:p.Ile646Asn
ENST00000646507.1:n.2034T>A
ENST00000391941.6:c.1865T>A	ENSP00000375805.2:p.Ile622Asn
ENST00000391942.6:n.1108T>A
ENST00000391944.7:c.1703T>A	ENSP00000375808.3:p.Ile568Asn
ENST00000391945.8:c.1937T>A	ENSP00000375809.3:p.Ile646Asn
ENST00000588652.5:n.2025T>A
NM_000400.3:c.1937T>A , LRG_461t1:c.1937T>A	NP_000391.1:p.Ile646Asn
XM_011526611.1:c.1859T>A	XP_011524913.1:p.Ile620Asn
XM_011526611.2:c.1859T>A	XP_011524913.1:p.Ile620Asn
XM_017026467.1:c.1814T>A	XP_016881956.1:p.Ile605Asn
XR_001753633.2:n.1984T>A
XR_001753634.2:n.1920T>A
NM_000400.4:c.1937T>A MANE Select	NP_000391.1:p.Ile646Asn