Canonical Allele Identifier: CA2338388724

Gene: ERCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352280T= , CM000681.2:g.45352280T=	GRCh38
NC_000019.9:g.45855538T= , CM000681.1:g.45855538T=	GRCh37
NC_000019.8:g.50547378T=	NCBI36
NG_007067.2:g.23308A= , LRG_461:g.23308A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.2119A=	ENSP00000375808.4:p.Asn707=
ENST00000682414.1:c.2119A=	ENSP00000507019.1:p.Asn707=
ENST00000682508.1:n.2148A=
ENST00000684218.1:c.*1377A=	ENSP00000507804.1:n.*1377A=
ENST00000684264.1:n.1675A=
ENST00000684407.1:c.1996A=	ENSP00000507775.1:p.Asn666=
ENST00000684458.1:c.*605A=	ENSP00000508260.1:n.*605A=
ENST00000684468.1:n.1831A=
ENST00000391945.10:c.2119A= MANE Select	ENSP00000375809.4:p.Asn707=
ENST00000646507.1:n.2216A=
ENST00000391941.6:c.2047A=	ENSP00000375805.2:p.Asn683=
ENST00000391942.6:n.1290A=
ENST00000391944.7:c.1885A=	ENSP00000375808.3:p.Asn629=
ENST00000391945.8:c.2119A=	ENSP00000375809.3:p.Asn707=
ENST00000588652.5:n.2207A=
NM_000400.3:c.2119A= , LRG_461t1:c.2119A=	NP_000391.1:p.Asn707=
XM_011526611.1:c.2041A=	XP_011524913.1:p.Asn681=
XM_011526611.2:c.2041A=	XP_011524913.1:p.Asn681=
XM_017026467.1:c.1996A=	XP_016881956.1:p.Asn666=
XR_001753633.2:n.2166A=
XR_001753634.2:n.2102A=
NM_000400.4:c.2119A= MANE Select	NP_000391.1:p.Asn707=