Canonical Allele Identifier: CA2338389058

Gene: ERCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352816A= , CM000681.2:g.45352816A=	GRCh38
NC_000019.9:g.45856074A= , CM000681.1:g.45856074A=	GRCh37
NC_000019.8:g.50547914A=	NCBI36
NG_007067.2:g.22772T= , LRG_461:g.22772T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1832T=	ENSP00000375808.4:p.Val611=
ENST00000682414.1:c.1832T=	ENSP00000507019.1:p.Val611=
ENST00000682508.1:n.1861T=
ENST00000684218.1:c.*1090T=	ENSP00000507804.1:n.*1090T=
ENST00000684264.1:n.1388T=
ENST00000684407.1:c.1709T=	ENSP00000507775.1:p.Val570=
ENST00000684458.1:c.*318T=	ENSP00000508260.1:n.*318T=
ENST00000684468.1:n.1544T=
ENST00000391945.10:c.1832T= MANE Select	ENSP00000375809.4:p.Val611=
ENST00000646507.1:n.1929T=
ENST00000391941.6:c.1760T=	ENSP00000375805.2:p.Val587=
ENST00000391942.6:n.1003T=
ENST00000391944.7:c.1598T=	ENSP00000375808.3:p.Val533=
ENST00000391945.8:c.1832T=	ENSP00000375809.3:p.Val611=
ENST00000588652.5:n.1920T=
NM_000400.3:c.1832T= , LRG_461t1:c.1832T=	NP_000391.1:p.Val611=
XM_011526611.1:c.1754T=	XP_011524913.1:p.Val585=
XM_011526611.2:c.1754T=	XP_011524913.1:p.Val585=
XM_017026467.1:c.1709T=	XP_016881956.1:p.Val570=
XR_001753633.2:n.1879T=
XR_001753634.2:n.1815T=
NM_000400.4:c.1832T= MANE Select	NP_000391.1:p.Val611=