Canonical Allele Identifier: CA2338388874

Gene: ERCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352525A= , CM000681.2:g.45352525A=	GRCh38
NC_000019.9:g.45855783A= , CM000681.1:g.45855783A=	GRCh37
NC_000019.8:g.50547623A=	NCBI36
NG_007067.2:g.23063T= , LRG_461:g.23063T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000391944.8:c.2027T=	ENSP00000375808.4:p.Leu676=
ENST00000682414.1:c.2027T=	ENSP00000507019.1:p.Leu676=
ENST00000682508.1:n.2056T=
ENST00000684218.1:c.*1285T=	ENSP00000507804.1:n.*1285T=
ENST00000684264.1:n.1583T=
ENST00000684407.1:c.1904T=	ENSP00000507775.1:p.Leu635=
ENST00000684458.1:c.*513T=	ENSP00000508260.1:n.*513T=
ENST00000684468.1:n.1739T=
ENST00000391945.10:c.2027T= MANE Select	ENSP00000375809.4:p.Leu676=
ENST00000646507.1:n.2124T=
ENST00000391941.6:c.1955T=	ENSP00000375805.2:p.Leu652=
ENST00000391942.6:n.1198T=
ENST00000391944.7:c.1793T=	ENSP00000375808.3:p.Leu598=
ENST00000391945.8:c.2027T=	ENSP00000375809.3:p.Leu676=
ENST00000588652.5:n.2115T=
NM_000400.3:c.2027T= , LRG_461t1:c.2027T=	NP_000391.1:p.Leu676=
XM_011526611.1:c.1949T=	XP_011524913.1:p.Leu650=
XM_011526611.2:c.1949T=	XP_011524913.1:p.Leu650=
XM_017026467.1:c.1904T=	XP_016881956.1:p.Leu635=
XR_001753633.2:n.2074T=
XR_001753634.2:n.2010T=
NM_000400.4:c.2027T= MANE Select	NP_000391.1:p.Leu676=