Canonical Allele Identifier: CA394824665

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14042081A>T (hg19) ; chr16:g.13948224A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948224A>T , CM000678.2:g.13948224A>T	GRCh38
NC_000016.9:g.14042081A>T , CM000678.1:g.14042081A>T	GRCh37
NC_000016.8:g.13949582A>T	NCBI36
NG_011442.1:g.33068A>T , LRG_463:g.33068A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2766A>T	ENSP00000507912.1:p.Leu922Phe
ENST00000683962.1:c.*2322A>T	ENSP00000506854.1:n.*2322A>T
ENST00000311895.8:c.2628A>T MANE Select	ENSP00000310520.7:p.Leu876Phe
ENST00000311895.7:c.2628A>T	ENSP00000310520.7:p.Leu876Phe
ENST00000389138.7:n.1905A>T
NM_005236.2:c.2628A>T , LRG_463t1:c.2628A>T	NP_005227.1:p.Leu876Phe
XM_011522424.1:c.2766A>T	XP_011520726.1:p.Leu922Phe
XM_011522425.1:c.2085A>T	XP_011520727.1:p.Leu695Phe
XM_011522426.1:c.1839A>T	XP_011520728.1:p.Leu613Phe
XM_011522427.1:c.1278A>T	XP_011520729.1:p.Leu426Phe
XR_932805.1:n.2787A>T
XM_011522424.3:c.2766A>T	XP_011520726.1:p.Leu922Phe
XM_017023043.2:c.1839A>T	XP_016878532.1:p.Leu613Phe
NM_005236.3:c.2628A>T MANE Select	NP_005227.1:p.Leu876Phe