Canonical Allele Identifier: CA394823144

Gene: ERCC4

Linked Data

• dbSNP Id: rs2141620565
• MyVariant Identifiers: chr16:g.14041803A>T (hg19) ; chr16:g.13947946A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947946A>T , CM000678.2:g.13947946A>T	GRCh38
NC_000016.9:g.14041803A>T , CM000678.1:g.14041803A>T	GRCh37
NC_000016.8:g.13949304A>T	NCBI36
NG_011442.1:g.32790A>T , LRG_463:g.32790A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2488A>T	ENSP00000507912.1:p.Ile830Phe
ENST00000683962.1:c.*2044A>T	ENSP00000506854.1:n.*2044A>T
ENST00000311895.8:c.2350A>T MANE Select	ENSP00000310520.7:p.Ile784Phe
ENST00000311895.7:c.2350A>T	ENSP00000310520.7:p.Ile784Phe
ENST00000389138.7:n.1627A>T
ENST00000462862.1:c.663A>T	ENSP00000461322.1:n.663A>T
NM_005236.2:c.2350A>T , LRG_463t1:c.2350A>T	NP_005227.1:p.Ile784Phe
XM_011522424.1:c.2488A>T	XP_011520726.1:p.Ile830Phe
XM_011522425.1:c.1807A>T	XP_011520727.1:p.Ile603Phe
XM_011522426.1:c.1561A>T	XP_011520728.1:p.Ile521Phe
XM_011522427.1:c.1000A>T	XP_011520729.1:p.Ile334Phe
XR_932805.1:n.2509A>T
XM_011522424.3:c.2488A>T	XP_011520726.1:p.Ile830Phe
XM_017023043.2:c.1561A>T	XP_016878532.1:p.Ile521Phe
NM_005236.3:c.2350A>T MANE Select	NP_005227.1:p.Ile784Phe