Canonical Allele Identifier: CA507818770

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45856052G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352794G>A , CM000681.2:g.45352794G>A	GRCh38
NC_000019.9:g.45856052G>A , CM000681.1:g.45856052G>A	GRCh37
NC_000019.8:g.50547892G>A	NCBI36
NG_007067.2:g.22794C>T , LRG_461:g.22794C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1854C>T	ENSP00000375808.4:p.Val618=
ENST00000682414.1:c.1854C>T	ENSP00000507019.1:p.Val618=
ENST00000682508.1:n.1883C>T
ENST00000684218.1:c.*1112C>T	ENSP00000507804.1:n.*1112C>T
ENST00000684264.1:n.1410C>T
ENST00000684407.1:c.1731C>T	ENSP00000507775.1:p.Val577=
ENST00000684458.1:c.*340C>T	ENSP00000508260.1:n.*340C>T
ENST00000684468.1:n.1566C>T
ENST00000391945.10:c.1854C>T MANE Select	ENSP00000375809.4:p.Val618=
ENST00000646507.1:n.1951C>T
ENST00000391941.6:c.1782C>T	ENSP00000375805.2:p.Val594=
ENST00000391942.6:n.1025C>T
ENST00000391944.7:c.1620C>T	ENSP00000375808.3:p.Val540=
ENST00000391945.8:c.1854C>T	ENSP00000375809.3:p.Val618=
ENST00000588652.5:n.1942C>T
NM_000400.3:c.1854C>T , LRG_461t1:c.1854C>T	NP_000391.1:p.Val618=
XM_011526611.1:c.1776C>T	XP_011524913.1:p.Val592=
XM_011526611.2:c.1776C>T	XP_011524913.1:p.Val592=
XM_017026467.1:c.1731C>T	XP_016881956.1:p.Val577=
XR_001753633.2:n.1901C>T
XR_001753634.2:n.1837C>T
NM_000400.4:c.1854C>T MANE Select	NP_000391.1:p.Val618=