Canonical Allele Identifier: CA507953397

Gene: ERCC2

Linked Data

• MyVariant Identifiers: chr19:g.45855869A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352611A>C , CM000681.2:g.45352611A>C	GRCh38
NC_000019.9:g.45855869A>C , CM000681.1:g.45855869A>C	GRCh37
NC_000019.8:g.50547709A>C	NCBI36
NG_007067.2:g.22977T>G , LRG_461:g.22977T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1941T>G	ENSP00000375808.4:p.Arg647=
ENST00000682414.1:c.1941T>G	ENSP00000507019.1:p.Arg647=
ENST00000682508.1:n.1970T>G
ENST00000684218.1:c.*1199T>G	ENSP00000507804.1:n.*1199T>G
ENST00000684264.1:n.1497T>G
ENST00000684407.1:c.1818T>G	ENSP00000507775.1:p.Arg606=
ENST00000684458.1:c.*427T>G	ENSP00000508260.1:n.*427T>G
ENST00000684468.1:n.1653T>G
ENST00000391945.10:c.1941T>G MANE Select	ENSP00000375809.4:p.Arg647=
ENST00000646507.1:n.2038T>G
ENST00000391941.6:c.1869T>G	ENSP00000375805.2:p.Arg623=
ENST00000391942.6:n.1112T>G
ENST00000391944.7:c.1707T>G	ENSP00000375808.3:p.Arg569=
ENST00000391945.8:c.1941T>G	ENSP00000375809.3:p.Arg647=
ENST00000588652.5:n.2029T>G
NM_000400.3:c.1941T>G , LRG_461t1:c.1941T>G	NP_000391.1:p.Arg647=
XM_011526611.1:c.1863T>G	XP_011524913.1:p.Arg621=
XM_011526611.2:c.1863T>G	XP_011524913.1:p.Arg621=
XM_017026467.1:c.1818T>G	XP_016881956.1:p.Arg606=
XR_001753633.2:n.1988T>G
XR_001753634.2:n.1924T>G
NM_000400.4:c.1941T>G MANE Select	NP_000391.1:p.Arg647=