Canonical Allele Identifier: CA2338388963

Gene: ERCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352667G= , CM000681.2:g.45352667G=	GRCh38
NC_000019.9:g.45855925G= , CM000681.1:g.45855925G=	GRCh37
NC_000019.8:g.50547765G=	NCBI36
NG_007067.2:g.22921C= , LRG_461:g.22921C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1903-18C=	ENSP00000375808.4:n.1903-18C=
ENST00000682414.1:c.1903-18C=	ENSP00000507019.1:n.1903-18C=
ENST00000682508.1:n.1932-18C=
ENST00000684218.1:c.*1161-18C=	ENSP00000507804.1:n.*1161-18C=
ENST00000684264.1:n.1459-18C=
ENST00000684407.1:c.1780-18C=	ENSP00000507775.1:n.1780-18C=
ENST00000684458.1:c.*389-18C=	ENSP00000508260.1:n.*389-18C=
ENST00000684468.1:n.1615-18C=
ENST00000391945.10:c.1903-18C= MANE Select	ENSP00000375809.4:n.1903-18C=
ENST00000646507.1:n.2000-18C=
ENST00000391941.6:c.1831-18C=	ENSP00000375805.2:n.1831-18C=
ENST00000391942.6:n.1074-18C=
ENST00000391944.7:c.1669-18C=	ENSP00000375808.3:n.1669-18C=
ENST00000391945.8:c.1903-18C=	ENSP00000375809.3:n.1903-18C=
ENST00000588652.5:n.1991-18C=
NM_000400.3:c.1903-18C= , LRG_461t1:c.1903-18C=	NP_000391.1:n.1903-18C=
XM_011526611.1:c.1825-18C=	XP_011524913.1:n.1825-18C=
XM_011526611.2:c.1825-18C=	XP_011524913.1:n.1825-18C=
XM_017026467.1:c.1780-18C=	XP_016881956.1:n.1780-18C=
XR_001753633.2:n.1950-18C=
XR_001753634.2:n.1886-18C=
NM_000400.4:c.1903-18C= MANE Select	NP_000391.1:n.1903-18C=