Canonical Allele Identifier: CA394824057

Gene: ERCC4

Linked Data

• dbSNP Id: rs2141620904
• COSMIC: COSM4166281
• MyVariant Identifiers: chr16:g.14041932A>T (hg19) ; chr16:g.13948075A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948075A>T , CM000678.2:g.13948075A>T	GRCh38
NC_000016.9:g.14041932A>T , CM000678.1:g.14041932A>T	GRCh37
NC_000016.8:g.13949433A>T	NCBI36
NG_011442.1:g.32919A>T , LRG_463:g.32919A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2617A>T	ENSP00000507912.1:p.Thr873Ser
ENST00000683962.1:c.*2173A>T	ENSP00000506854.1:n.*2173A>T
ENST00000311895.8:c.2479A>T MANE Select	ENSP00000310520.7:p.Thr827Ser
ENST00000311895.7:c.2479A>T	ENSP00000310520.7:p.Thr827Ser
ENST00000389138.7:n.1756A>T
NM_005236.2:c.2479A>T , LRG_463t1:c.2479A>T	NP_005227.1:p.Thr827Ser
XM_011522424.1:c.2617A>T	XP_011520726.1:p.Thr873Ser
XM_011522425.1:c.1936A>T	XP_011520727.1:p.Thr646Ser
XM_011522426.1:c.1690A>T	XP_011520728.1:p.Thr564Ser
XM_011522427.1:c.1129A>T	XP_011520729.1:p.Thr377Ser
XR_932805.1:n.2638A>T
XM_011522424.3:c.2617A>T	XP_011520726.1:p.Thr873Ser
XM_017023043.2:c.1690A>T	XP_016878532.1:p.Thr564Ser
NM_005236.3:c.2479A>T MANE Select	NP_005227.1:p.Thr827Ser