Canonical Allele Identifier: CA2338389858

Gene: ERCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45353996C= , CM000681.2:g.45353996C=	GRCh38
NC_000019.9:g.45857254C= , CM000681.1:g.45857254C=	GRCh37
NC_000019.8:g.50549094C=	NCBI36
NG_007067.2:g.21592G= , LRG_461:g.21592G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000391944.8:c.1666-662G=	ENSP00000375808.4:n.1666-662G=
ENST00000682414.1:c.1666-662G=	ENSP00000507019.1:n.1666-662G=
ENST00000682508.1:n.1695-662G=
ENST00000684218.1:c.*924-662G=	ENSP00000507804.1:n.*924-662G=
ENST00000684264.1:n.1222-662G=
ENST00000684407.1:c.1543-662G=	ENSP00000507775.1:n.1543-662G=
ENST00000684458.1:c.*152-662G=	ENSP00000508260.1:n.*152-662G=
ENST00000684468.1:n.1378-662G=
ENST00000391945.10:c.1666-662G= MANE Select	ENSP00000375809.4:n.1666-662G=
ENST00000587376.6:c.725-662G=
ENST00000646507.1:n.1763-662G=
ENST00000391941.6:c.1594-662G=	ENSP00000375805.2:n.1594-662G=
ENST00000391942.6:n.837-662G=
ENST00000391944.7:c.1432-662G=	ENSP00000375808.3:n.1432-662G=
ENST00000391945.8:c.1666-662G=	ENSP00000375809.3:n.1666-662G=
ENST00000587376.5:c.725-662G=
ENST00000588652.5:n.1754-662G=
NM_000400.3:c.1666-662G= , LRG_461t1:c.1666-662G=	NP_000391.1:n.1666-662G=
XM_011526611.1:c.1588-662G=	XP_011524913.1:n.1588-662G=
XR_935763.1:n.1649-662G=
XM_011526611.2:c.1588-662G=	XP_011524913.1:n.1588-662G=
XM_017026467.1:c.1543-662G=	XP_016881956.1:n.1543-662G=
XR_001753633.2:n.1713-662G=
XR_001753634.2:n.1649-662G=
NM_000400.4:c.1666-662G= MANE Select	NP_000391.1:n.1666-662G=