Canonical Allele Identifier: CA394812280

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029453A>T (hg19) ; chr16:g.13935596A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935596A>T , CM000678.2:g.13935596A>T	GRCh38
NC_000016.9:g.14029453A>T , CM000678.1:g.14029453A>T	GRCh37
NC_000016.8:g.13936954A>T	NCBI36
NG_011442.1:g.20440A>T , LRG_463:g.20440A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1742A>T
ENST00000682617.1:c.1802A>T	ENSP00000507912.1:p.His601Leu
ENST00000682826.1:c.*978A>T	ENSP00000507274.1:n.*978A>T
ENST00000682909.1:n.3704A>T
ENST00000683277.1:n.3309A>T
ENST00000683407.1:n.1672A>T
ENST00000683962.1:c.*1358A>T	ENSP00000506854.1:n.*1358A>T
ENST00000311895.8:c.1664A>T MANE Select	ENSP00000310520.7:p.His555Leu
ENST00000311895.7:c.1664A>T	ENSP00000310520.7:p.His555Leu
ENST00000389138.7:n.941A>T
NM_005236.2:c.1664A>T , LRG_463t1:c.1664A>T	NP_005227.1:p.His555Leu
XM_011522424.1:c.1802A>T	XP_011520726.1:p.His601Leu
XM_011522425.1:c.1121A>T	XP_011520727.1:p.His374Leu
XM_011522426.1:c.875A>T	XP_011520728.1:p.His292Leu
XM_011522427.1:c.314A>T	XP_011520729.1:p.His105Leu
XR_932805.1:n.1823A>T
XM_011522424.3:c.1802A>T	XP_011520726.1:p.His601Leu
XM_017023043.2:c.875A>T	XP_016878532.1:p.His292Leu
NM_005236.3:c.1664A>T MANE Select	NP_005227.1:p.His555Leu