Canonical Allele Identifier: CA507953349

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45855770G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352512G>C , CM000681.2:g.45352512G>C	GRCh38
NC_000019.9:g.45855770G>C , CM000681.1:g.45855770G>C	GRCh37
NC_000019.8:g.50547610G>C	NCBI36
NG_007067.2:g.23076C>G , LRG_461:g.23076C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000391944.8:c.2040C>G	ENSP00000375808.4:p.Ala680=
ENST00000682414.1:c.2040C>G	ENSP00000507019.1:p.Ala680=
ENST00000682508.1:n.2069C>G
ENST00000684218.1:c.*1298C>G	ENSP00000507804.1:n.*1298C>G
ENST00000684264.1:n.1596C>G
ENST00000684407.1:c.1917C>G	ENSP00000507775.1:p.Ala639=
ENST00000684458.1:c.*526C>G	ENSP00000508260.1:n.*526C>G
ENST00000684468.1:n.1752C>G
ENST00000391945.10:c.2040C>G MANE Select	ENSP00000375809.4:p.Ala680=
ENST00000646507.1:n.2137C>G
ENST00000391941.6:c.1968C>G	ENSP00000375805.2:p.Ala656=
ENST00000391942.6:n.1211C>G
ENST00000391944.7:c.1806C>G	ENSP00000375808.3:p.Ala602=
ENST00000391945.8:c.2040C>G	ENSP00000375809.3:p.Ala680=
ENST00000588652.5:n.2128C>G
NM_000400.3:c.2040C>G , LRG_461t1:c.2040C>G	NP_000391.1:p.Ala680=
XM_011526611.1:c.1962C>G	XP_011524913.1:p.Ala654=
XM_011526611.2:c.1962C>G	XP_011524913.1:p.Ala654=
XM_017026467.1:c.1917C>G	XP_016881956.1:p.Ala639=
XR_001753633.2:n.2087C>G
XR_001753634.2:n.2023C>G
NM_000400.4:c.2040C>G MANE Select	NP_000391.1:p.Ala680=