Canonical Allele Identifier: CA2209081536

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13945011T= , CM000678.2:g.13945011T=	GRCh38
NC_000016.9:g.14038868T= , CM000678.1:g.14038868T=	GRCh37
NC_000016.8:g.13946369T=	NCBI36
NG_011442.1:g.29855T= , LRG_463:g.29855T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2155+176T=	ENSP00000507912.1:n.2155+176T=
ENST00000683962.1:c.*1711+176T=	ENSP00000506854.1:n.*1711+176T=
ENST00000311895.8:c.2017+176T= MANE Select	ENSP00000310520.7:n.2017+176T=
ENST00000311895.7:c.2017+176T=	ENSP00000310520.7:n.2017+176T=
ENST00000389138.7:n.1294+176T=
ENST00000462862.1:c.330+176T=	ENSP00000461322.1:n.330+176T=
NM_005236.2:c.2017+176T= , LRG_463t1:c.2017+176T=	NP_005227.1:n.2017+176T=
XM_011522424.1:c.2155+176T=	XP_011520726.1:n.2155+176T=
XM_011522425.1:c.1474+176T=	XP_011520727.1:n.1474+176T=
XM_011522426.1:c.1228+176T=	XP_011520728.1:n.1228+176T=
XM_011522427.1:c.667+176T=	XP_011520729.1:n.667+176T=
XR_932805.1:n.2176+176T=
XM_011522424.3:c.2155+176T=	XP_011520726.1:n.2155+176T=
XM_017023043.2:c.1228+176T=	XP_016878532.1:n.1228+176T=
NM_005236.3:c.2017+176T= MANE Select	NP_005227.1:n.2017+176T=