Canonical Allele Identifier: CA394817470

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14038605G>T (hg19) ; chr16:g.13944748G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13944748G>T , CM000678.2:g.13944748G>T	GRCh38
NC_000016.9:g.14038605G>T , CM000678.1:g.14038605G>T	GRCh37
NC_000016.8:g.13946106G>T	NCBI36
NG_011442.1:g.29592G>T , LRG_463:g.29592G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2068G>T	ENSP00000507912.1:p.Glu690Ter
ENST00000683962.1:c.*1624G>T	ENSP00000506854.1:n.*1624G>T
ENST00000311895.8:c.1930G>T MANE Select	ENSP00000310520.7:p.Glu644Ter
ENST00000311895.7:c.1930G>T	ENSP00000310520.7:p.Glu644Ter
ENST00000389138.7:n.1207G>T
ENST00000462862.1:c.243G>T	ENSP00000461322.1:n.243G>T
NM_005236.2:c.1930G>T , LRG_463t1:c.1930G>T	NP_005227.1:p.Glu644Ter
XM_011522424.1:c.2068G>T	XP_011520726.1:p.Glu690Ter
XM_011522425.1:c.1387G>T	XP_011520727.1:p.Glu463Ter
XM_011522426.1:c.1141G>T	XP_011520728.1:p.Glu381Ter
XM_011522427.1:c.580G>T	XP_011520729.1:p.Glu194Ter
XR_932805.1:n.2089G>T
XM_011522424.3:c.2068G>T	XP_011520726.1:p.Glu690Ter
XM_017023043.2:c.1141G>T	XP_016878532.1:p.Glu381Ter
NM_005236.3:c.1930G>T MANE Select	NP_005227.1:p.Glu644Ter