Canonical Allele Identifier: CA2338388929

Gene: ERCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352613G= , CM000681.2:g.45352613G=	GRCh38
NC_000019.9:g.45855871G= , CM000681.1:g.45855871G=	GRCh37
NC_000019.8:g.50547711G=	NCBI36
NG_007067.2:g.22975C= , LRG_461:g.22975C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1939C=	ENSP00000375808.4:p.Arg647=
ENST00000682414.1:c.1939C=	ENSP00000507019.1:p.Arg647=
ENST00000682508.1:n.1968C=
ENST00000684218.1:c.*1197C=	ENSP00000507804.1:n.*1197C=
ENST00000684264.1:n.1495C=
ENST00000684407.1:c.1816C=	ENSP00000507775.1:p.Arg606=
ENST00000684458.1:c.*425C=	ENSP00000508260.1:n.*425C=
ENST00000684468.1:n.1651C=
ENST00000391945.10:c.1939C= MANE Select	ENSP00000375809.4:p.Arg647=
ENST00000646507.1:n.2036C=
ENST00000391941.6:c.1867C=	ENSP00000375805.2:p.Arg623=
ENST00000391942.6:n.1110C=
ENST00000391944.7:c.1705C=	ENSP00000375808.3:p.Arg569=
ENST00000391945.8:c.1939C=	ENSP00000375809.3:p.Arg647=
ENST00000588652.5:n.2027C=
NM_000400.3:c.1939C= , LRG_461t1:c.1939C=	NP_000391.1:p.Arg647=
XM_011526611.1:c.1861C=	XP_011524913.1:p.Arg621=
XM_011526611.2:c.1861C=	XP_011524913.1:p.Arg621=
XM_017026467.1:c.1816C=	XP_016881956.1:p.Arg606=
XR_001753633.2:n.1986C=
XR_001753634.2:n.1922C=
NM_000400.4:c.1939C= MANE Select	NP_000391.1:p.Arg647=