Canonical Allele Identifier: CA2338388691

Gene: ERCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352244A= , CM000681.2:g.45352244A=	GRCh38
NC_000019.9:g.45855502A= , CM000681.1:g.45855502A=	GRCh37
NC_000019.8:g.50547342A=	NCBI36
NG_007067.2:g.23344T= , LRG_461:g.23344T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000391944.8:c.2155T=	ENSP00000375808.4:p.Tyr719=
ENST00000682414.1:c.2155T=	ENSP00000507019.1:p.Tyr719=
ENST00000682508.1:n.2184T=
ENST00000684218.1:c.*1413T=	ENSP00000507804.1:n.*1413T=
ENST00000684264.1:n.1711T=
ENST00000684407.1:c.2032T=	ENSP00000507775.1:p.Tyr678=
ENST00000684458.1:c.*641T=	ENSP00000508260.1:n.*641T=
ENST00000684468.1:n.1867T=
ENST00000391945.10:c.2155T= MANE Select	ENSP00000375809.4:p.Tyr719=
ENST00000646507.1:n.2252T=
ENST00000391941.6:c.2083T=	ENSP00000375805.2:p.Tyr695=
ENST00000391942.6:n.1326T=
ENST00000391944.7:c.1921T=	ENSP00000375808.3:p.Tyr641=
ENST00000391945.8:c.2155T=	ENSP00000375809.3:p.Tyr719=
ENST00000588652.5:n.2243T=
NM_000400.3:c.2155T= , LRG_461t1:c.2155T=	NP_000391.1:p.Tyr719=
XM_011526611.1:c.2077T=	XP_011524913.1:p.Tyr693=
XM_011526611.2:c.2077T=	XP_011524913.1:p.Tyr693=
XM_017026467.1:c.2032T=	XP_016881956.1:p.Tyr678=
XR_001753633.2:n.2202T=
XR_001753634.2:n.2138T=
NM_000400.4:c.2155T= MANE Select	NP_000391.1:p.Tyr719=