Canonical Allele Identifier: CA394824497

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14042031G>T (hg19) ; chr16:g.13948174G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948174G>T , CM000678.2:g.13948174G>T	GRCh38
NC_000016.9:g.14042031G>T , CM000678.1:g.14042031G>T	GRCh37
NC_000016.8:g.13949532G>T	NCBI36
NG_011442.1:g.33018G>T , LRG_463:g.33018G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2716G>T	ENSP00000507912.1:p.Ala906Ser
ENST00000683962.1:c.*2272G>T	ENSP00000506854.1:n.*2272G>T
ENST00000311895.8:c.2578G>T MANE Select	ENSP00000310520.7:p.Ala860Ser
ENST00000311895.7:c.2578G>T	ENSP00000310520.7:p.Ala860Ser
ENST00000389138.7:n.1855G>T
NM_005236.2:c.2578G>T , LRG_463t1:c.2578G>T	NP_005227.1:p.Ala860Ser
XM_011522424.1:c.2716G>T	XP_011520726.1:p.Ala906Ser
XM_011522425.1:c.2035G>T	XP_011520727.1:p.Ala679Ser
XM_011522426.1:c.1789G>T	XP_011520728.1:p.Ala597Ser
XM_011522427.1:c.1228G>T	XP_011520729.1:p.Ala410Ser
XR_932805.1:n.2737G>T
XM_011522424.3:c.2716G>T	XP_011520726.1:p.Ala906Ser
XM_017023043.2:c.1789G>T	XP_016878532.1:p.Ala597Ser
NM_005236.3:c.2578G>T MANE Select	NP_005227.1:p.Ala860Ser