Canonical Allele Identifier: CA394812626

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029545A>T (hg19) ; chr16:g.13935688A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935688A>T , CM000678.2:g.13935688A>T	GRCh38
NC_000016.9:g.14029545A>T , CM000678.1:g.14029545A>T	GRCh37
NC_000016.8:g.13937046A>T	NCBI36
NG_011442.1:g.20532A>T , LRG_463:g.20532A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1834A>T
ENST00000682617.1:c.1894A>T	ENSP00000507912.1:p.Thr632Ser
ENST00000682826.1:c.*1070A>T	ENSP00000507274.1:n.*1070A>T
ENST00000682909.1:n.3796A>T
ENST00000683277.1:n.3401A>T
ENST00000683407.1:n.1764A>T
ENST00000683962.1:c.*1450A>T	ENSP00000506854.1:n.*1450A>T
ENST00000311895.8:c.1756A>T MANE Select	ENSP00000310520.7:p.Thr586Ser
ENST00000311895.7:c.1756A>T	ENSP00000310520.7:p.Thr586Ser
ENST00000389138.7:n.1033A>T
NM_005236.2:c.1756A>T , LRG_463t1:c.1756A>T	NP_005227.1:p.Thr586Ser
XM_011522424.1:c.1894A>T	XP_011520726.1:p.Thr632Ser
XM_011522425.1:c.1213A>T	XP_011520727.1:p.Thr405Ser
XM_011522426.1:c.967A>T	XP_011520728.1:p.Thr323Ser
XM_011522427.1:c.406A>T	XP_011520729.1:p.Thr136Ser
XR_932805.1:n.1915A>T
XM_011522424.3:c.1894A>T	XP_011520726.1:p.Thr632Ser
XM_017023043.2:c.967A>T	XP_016878532.1:p.Thr323Ser
NM_005236.3:c.1756A>T MANE Select	NP_005227.1:p.Thr586Ser