Canonical Allele Identifier: CA394822291

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14041621G>T (hg19) ; chr16:g.13947764G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947764G>T , CM000678.2:g.13947764G>T	GRCh38
NC_000016.9:g.14041621G>T , CM000678.1:g.14041621G>T	GRCh37
NC_000016.8:g.13949122G>T	NCBI36
NG_011442.1:g.32608G>T , LRG_463:g.32608G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2306G>T	ENSP00000507912.1:p.Cys769Phe
ENST00000683962.1:c.*1862G>T	ENSP00000506854.1:n.*1862G>T
ENST00000311895.8:c.2168G>T MANE Select	ENSP00000310520.7:p.Cys723Phe
ENST00000311895.7:c.2168G>T	ENSP00000310520.7:p.Cys723Phe
ENST00000389138.7:n.1445G>T
ENST00000462862.1:c.481G>T	ENSP00000461322.1:n.481G>T
NM_005236.2:c.2168G>T , LRG_463t1:c.2168G>T	NP_005227.1:p.Cys723Phe
XM_011522424.1:c.2306G>T	XP_011520726.1:p.Cys769Phe
XM_011522425.1:c.1625G>T	XP_011520727.1:p.Cys542Phe
XM_011522426.1:c.1379G>T	XP_011520728.1:p.Cys460Phe
XM_011522427.1:c.818G>T	XP_011520729.1:p.Cys273Phe
XR_932805.1:n.2327G>T
XM_011522424.3:c.2306G>T	XP_011520726.1:p.Cys769Phe
XM_017023043.2:c.1379G>T	XP_016878532.1:p.Cys460Phe
NM_005236.3:c.2168G>T MANE Select	NP_005227.1:p.Cys723Phe