Canonical Allele Identifier: CA2338388739

Gene: ERCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352313A= , CM000681.2:g.45352313A=	GRCh38
NC_000019.9:g.45855571A= , CM000681.1:g.45855571A=	GRCh37
NC_000019.8:g.50547411A=	NCBI36
NG_007067.2:g.23275T= , LRG_461:g.23275T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.2086T=	ENSP00000375808.4:p.Trp696=
ENST00000682414.1:c.2086T=	ENSP00000507019.1:p.Trp696=
ENST00000682508.1:n.2115T=
ENST00000684218.1:c.*1344T=	ENSP00000507804.1:n.*1344T=
ENST00000684264.1:n.1642T=
ENST00000684407.1:c.1963T=	ENSP00000507775.1:p.Trp655=
ENST00000684458.1:c.*572T=	ENSP00000508260.1:n.*572T=
ENST00000684468.1:n.1798T=
ENST00000391945.10:c.2086T= MANE Select	ENSP00000375809.4:p.Trp696=
ENST00000646507.1:n.2183T=
ENST00000391941.6:c.2014T=	ENSP00000375805.2:p.Trp672=
ENST00000391942.6:n.1257T=
ENST00000391944.7:c.1852T=	ENSP00000375808.3:p.Trp618=
ENST00000391945.8:c.2086T=	ENSP00000375809.3:p.Trp696=
ENST00000588652.5:n.2174T=
NM_000400.3:c.2086T= , LRG_461t1:c.2086T=	NP_000391.1:p.Trp696=
XM_011526611.1:c.2008T=	XP_011524913.1:p.Trp670=
XM_011526611.2:c.2008T=	XP_011524913.1:p.Trp670=
XM_017026467.1:c.1963T=	XP_016881956.1:p.Trp655=
XR_001753633.2:n.2133T=
XR_001753634.2:n.2069T=
NM_000400.4:c.2086T= MANE Select	NP_000391.1:p.Trp696=