Canonical Allele Identifier: CA2338388727

Gene: ERCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352285T= , CM000681.2:g.45352285T=	GRCh38
NC_000019.9:g.45855543T= , CM000681.1:g.45855543T=	GRCh37
NC_000019.8:g.50547383T=	NCBI36
NG_007067.2:g.23303A= , LRG_461:g.23303A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.2114A=	ENSP00000375808.4:p.Asn705=
ENST00000682414.1:c.2114A=	ENSP00000507019.1:p.Asn705=
ENST00000682508.1:n.2143A=
ENST00000684218.1:c.*1372A=	ENSP00000507804.1:n.*1372A=
ENST00000684264.1:n.1670A=
ENST00000684407.1:c.1991A=	ENSP00000507775.1:p.Asn664=
ENST00000684458.1:c.*600A=	ENSP00000508260.1:n.*600A=
ENST00000684468.1:n.1826A=
ENST00000391945.10:c.2114A= MANE Select	ENSP00000375809.4:p.Asn705=
ENST00000646507.1:n.2211A=
ENST00000391941.6:c.2042A=	ENSP00000375805.2:p.Asn681=
ENST00000391942.6:n.1285A=
ENST00000391944.7:c.1880A=	ENSP00000375808.3:p.Asn627=
ENST00000391945.8:c.2114A=	ENSP00000375809.3:p.Asn705=
ENST00000588652.5:n.2202A=
NM_000400.3:c.2114A= , LRG_461t1:c.2114A=	NP_000391.1:p.Asn705=
XM_011526611.1:c.2036A=	XP_011524913.1:p.Asn679=
XM_011526611.2:c.2036A=	XP_011524913.1:p.Asn679=
XM_017026467.1:c.1991A=	XP_016881956.1:p.Asn664=
XR_001753633.2:n.2161A=
XR_001753634.2:n.2097A=
NM_000400.4:c.2114A= MANE Select	NP_000391.1:p.Asn705=