Canonical Allele Identifier: CA2338391657

Gene: ERCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45357215C= , CM000681.2:g.45357215C=	GRCh38
NC_000019.9:g.45860473C= , CM000681.1:g.45860473C=	GRCh37
NC_000019.8:g.50552313C=	NCBI36
NG_007067.2:g.18373G= , LRG_461:g.18373G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000391944.8:c.1479+55G=	ENSP00000375808.4:n.1479+55G=
ENST00000682414.1:c.1479+55G=	ENSP00000507019.1:n.1479+55G=
ENST00000682508.1:n.1508+55G=
ENST00000684218.1:c.*737+55G=	ENSP00000507804.1:n.*737+55G=
ENST00000684264.1:n.1035+55G=
ENST00000684407.1:c.1356+55G=	ENSP00000507775.1:n.1356+55G=
ENST00000684458.1:c.*29+55G=	ENSP00000508260.1:n.*29+55G=
ENST00000684468.1:n.1255+55G=
ENST00000391945.10:c.1479+55G= MANE Select	ENSP00000375809.4:n.1479+55G=
ENST00000587376.6:c.602+55G=
ENST00000646507.1:n.1576+55G=
ENST00000391941.6:c.1407+55G=	ENSP00000375805.2:n.1407+55G=
ENST00000391942.6:n.650+55G=
ENST00000391944.7:c.1245+55G=	ENSP00000375808.3:n.1245+55G=
ENST00000391945.8:c.1479+55G=	ENSP00000375809.3:n.1479+55G=
ENST00000587376.5:c.602+55G=
ENST00000588652.5:n.1567+55G=
NM_000400.3:c.1479+55G= , LRG_461t1:c.1479+55G=	NP_000391.1:n.1479+55G=
XM_011526611.1:c.1401+55G=	XP_011524913.1:n.1401+55G=
XR_935763.1:n.1526+55G=
XM_011526611.2:c.1401+55G=	XP_011524913.1:n.1401+55G=
XM_017026467.1:c.1356+55G=	XP_016881956.1:n.1356+55G=
XR_001753633.2:n.1526+55G=
XR_001753634.2:n.1526+55G=
NM_000400.4:c.1479+55G= MANE Select	NP_000391.1:n.1479+55G=