Canonical Allele Identifier: CA2338388689

Gene: ERCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352241A= , CM000681.2:g.45352241A=	GRCh38
NC_000019.9:g.45855499A= , CM000681.1:g.45855499A=	GRCh37
NC_000019.8:g.50547339A=	NCBI36
NG_007067.2:g.23347T= , LRG_461:g.23347T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000391944.8:c.2158T=	ENSP00000375808.4:p.Phe720=
ENST00000682414.1:c.2158T=	ENSP00000507019.1:p.Phe720=
ENST00000682508.1:n.2187T=
ENST00000684218.1:c.*1416T=	ENSP00000507804.1:n.*1416T=
ENST00000684264.1:n.1714T=
ENST00000684407.1:c.2035T=	ENSP00000507775.1:p.Phe679=
ENST00000684458.1:c.*644T=	ENSP00000508260.1:n.*644T=
ENST00000684468.1:n.1870T=
ENST00000391945.10:c.2158T= MANE Select	ENSP00000375809.4:p.Phe720=
ENST00000646507.1:n.2255T=
ENST00000391941.6:c.2086T=	ENSP00000375805.2:p.Phe696=
ENST00000391942.6:n.1329T=
ENST00000391944.7:c.1924T=	ENSP00000375808.3:p.Phe642=
ENST00000391945.8:c.2158T=	ENSP00000375809.3:p.Phe720=
ENST00000588652.5:n.2246T=
NM_000400.3:c.2158T= , LRG_461t1:c.2158T=	NP_000391.1:p.Phe720=
XM_011526611.1:c.2080T=	XP_011524913.1:p.Phe694=
XM_011526611.2:c.2080T=	XP_011524913.1:p.Phe694=
XM_017026467.1:c.2035T=	XP_016881956.1:p.Phe679=
XR_001753633.2:n.2205T=
XR_001753634.2:n.2141T=
NM_000400.4:c.2158T= MANE Select	NP_000391.1:p.Phe720=