Canonical Allele Identifier: CA2338395601

Gene: ERCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45363890C= , CM000681.2:g.45363890C=	GRCh38
NC_000019.9:g.45867148C= , CM000681.1:g.45867148C=	GRCh37
NC_000019.8:g.50558988C=	NCBI36
NG_007067.2:g.11698G= , LRG_461:g.11698G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.971G=	ENSP00000375808.4:p.Arg324=
ENST00000682414.1:c.971G=	ENSP00000507019.1:p.Arg324=
ENST00000682508.1:n.1000G=
ENST00000684218.1:c.*229G=	ENSP00000507804.1:n.*229G=
ENST00000684407.1:c.848G=	ENSP00000507775.1:p.Arg283=
ENST00000684458.1:c.971G=	ENSP00000508260.1:p.Arg324=
ENST00000391945.10:c.971G= MANE Select	ENSP00000375809.4:p.Arg324=
ENST00000587376.6:c.94G=
ENST00000646507.1:n.1068G=
ENST00000391941.6:c.899G=	ENSP00000375805.2:p.Arg300=
ENST00000391944.7:c.737G=	ENSP00000375808.3:p.Arg246=
ENST00000391945.8:c.971G=	ENSP00000375809.3:p.Arg324=
ENST00000485403.6:c.899G=	ENSP00000431229.2:p.Arg300=
ENST00000587376.5:c.94G=
NM_000400.3:c.971G= , LRG_461t1:c.971G=	NP_000391.1:p.Arg324=
NM_001130867.1:c.899G=	NP_001124339.1:p.Arg300=
XM_011526611.1:c.893G=	XP_011524913.1:p.Arg298=
XR_935763.1:n.1018G=
XM_011526611.2:c.893G=	XP_011524913.1:p.Arg298=
XM_017026467.1:c.848G=	XP_016881956.1:p.Arg283=
XR_001753633.2:n.1018G=
XR_001753634.2:n.1018G=
NM_000400.4:c.971G= MANE Select	NP_000391.1:p.Arg324=
NM_001130867.2:c.899G=	NP_001124339.1:p.Arg300=