Canonical Allele Identifier: CA2338388712

Gene: ERCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352267T= , CM000681.2:g.45352267T=	GRCh38
NC_000019.9:g.45855525T= , CM000681.1:g.45855525T=	GRCh37
NC_000019.8:g.50547365T=	NCBI36
NG_007067.2:g.23321A= , LRG_461:g.23321A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.2132A=	ENSP00000375808.4:p.Asp711=
ENST00000682414.1:c.2132A=	ENSP00000507019.1:p.Asp711=
ENST00000682508.1:n.2161A=
ENST00000684218.1:c.*1390A=	ENSP00000507804.1:n.*1390A=
ENST00000684264.1:n.1688A=
ENST00000684407.1:c.2009A=	ENSP00000507775.1:p.Asp670=
ENST00000684458.1:c.*618A=	ENSP00000508260.1:n.*618A=
ENST00000684468.1:n.1844A=
ENST00000391945.10:c.2132A= MANE Select	ENSP00000375809.4:p.Asp711=
ENST00000646507.1:n.2229A=
ENST00000391941.6:c.2060A=	ENSP00000375805.2:p.Asp687=
ENST00000391942.6:n.1303A=
ENST00000391944.7:c.1898A=	ENSP00000375808.3:p.Asp633=
ENST00000391945.8:c.2132A=	ENSP00000375809.3:p.Asp711=
ENST00000588652.5:n.2220A=
NM_000400.3:c.2132A= , LRG_461t1:c.2132A=	NP_000391.1:p.Asp711=
XM_011526611.1:c.2054A=	XP_011524913.1:p.Asp685=
XM_011526611.2:c.2054A=	XP_011524913.1:p.Asp685=
XM_017026467.1:c.2009A=	XP_016881956.1:p.Asp670=
XR_001753633.2:n.2179A=
XR_001753634.2:n.2115A=
NM_000400.4:c.2132A= MANE Select	NP_000391.1:p.Asp711=