Canonical Allele Identifier: CA2338389030

Gene: ERCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352772C= , CM000681.2:g.45352772C=	GRCh38
NC_000019.9:g.45856030C= , CM000681.1:g.45856030C=	GRCh37
NC_000019.8:g.50547870C=	NCBI36
NG_007067.2:g.22816G= , LRG_461:g.22816G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1876G=	ENSP00000375808.4:p.Val626=
ENST00000682414.1:c.1876G=	ENSP00000507019.1:p.Val626=
ENST00000682508.1:n.1905G=
ENST00000684218.1:c.*1134G=	ENSP00000507804.1:n.*1134G=
ENST00000684264.1:n.1432G=
ENST00000684407.1:c.1753G=	ENSP00000507775.1:p.Val585=
ENST00000684458.1:c.*362G=	ENSP00000508260.1:n.*362G=
ENST00000684468.1:n.1588G=
ENST00000391945.10:c.1876G= MANE Select	ENSP00000375809.4:p.Val626=
ENST00000646507.1:n.1973G=
ENST00000391941.6:c.1804G=	ENSP00000375805.2:p.Val602=
ENST00000391942.6:n.1047G=
ENST00000391944.7:c.1642G=	ENSP00000375808.3:p.Val548=
ENST00000391945.8:c.1876G=	ENSP00000375809.3:p.Val626=
ENST00000588652.5:n.1964G=
NM_000400.3:c.1876G= , LRG_461t1:c.1876G=	NP_000391.1:p.Val626=
XM_011526611.1:c.1798G=	XP_011524913.1:p.Val600=
XM_011526611.2:c.1798G=	XP_011524913.1:p.Val600=
XM_017026467.1:c.1753G=	XP_016881956.1:p.Val585=
XR_001753633.2:n.1923G=
XR_001753634.2:n.1859G=
NM_000400.4:c.1876G= MANE Select	NP_000391.1:p.Val626=