Canonical Allele Identifier: CA278482629

Gene: ERCC4

Linked Data

• dbSNP Id: rs200317919
• gnomAD v4: 16-13944818-C-T
• MyVariant Identifiers: chr16:g.14038675C>T (hg19) ; chr16:g.13944818C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13944818C>T , CM000678.2:g.13944818C>T	GRCh38
NC_000016.9:g.14038675C>T , CM000678.1:g.14038675C>T	GRCh37
NC_000016.8:g.13946176C>T	NCBI36
NG_011442.1:g.29662C>T , LRG_463:g.29662C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2138C>T	ENSP00000507912.1:p.Thr713Ile
ENST00000683962.1:c.*1694C>T	ENSP00000506854.1:n.*1694C>T
ENST00000311895.8:c.2000C>T MANE Select	ENSP00000310520.7:p.Thr667Ile
ENST00000311895.7:c.2000C>T	ENSP00000310520.7:p.Thr667Ile
ENST00000389138.7:n.1277C>T
ENST00000462862.1:c.313C>T	ENSP00000461322.1:n.313C>T
NM_005236.2:c.2000C>T , LRG_463t1:c.2000C>T	NP_005227.1:p.Thr667Ile
XM_011522424.1:c.2138C>T	XP_011520726.1:p.Thr713Ile
XM_011522425.1:c.1457C>T	XP_011520727.1:p.Thr486Ile
XM_011522426.1:c.1211C>T	XP_011520728.1:p.Thr404Ile
XM_011522427.1:c.650C>T	XP_011520729.1:p.Thr217Ile
XR_932805.1:n.2159C>T
XM_011522424.3:c.2138C>T	XP_011520726.1:p.Thr713Ile
XM_017023043.2:c.1211C>T	XP_016878532.1:p.Thr404Ile
NM_005236.3:c.2000C>T MANE Select	NP_005227.1:p.Thr667Ile