Canonical Allele Identifier: CA2631831497

Gene: ERCC4

Linked Data

• gnomAD v4: 16-13948495-TCTCTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948496_13948500del , CM000678.2:g.13948496_13948500del	GRCh38
NC_000016.9:g.14042353_14042357del , CM000678.1:g.14042353_14042357del	GRCh37
NC_000016.8:g.13949854_13949858del	NCBI36
NG_011442.1:g.33340_33344del , LRG_463:g.33340_33344del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.*149_*153del	ENSP00000507912.1:n.*149_*153del
ENST00000683962.1:c.*2594_*2598del	ENSP00000506854.1:n.*2594_*2598del
ENST00000311895.8:c.*149_*153del MANE Select	ENSP00000310520.7:n.*149_*153del
ENST00000311895.7:c.*149_*153del	ENSP00000310520.7:n.*149_*153del
NM_005236.2:c.*149_*153del , LRG_463t1:c.*149_*153del	NP_005227.1:n.*149_*153del
XM_011522424.1:c.*149_*153del	XP_011520726.1:n.*149_*153del
XM_011522425.1:c.*149_*153del	XP_011520727.1:n.*149_*153del
XM_011522426.1:c.*149_*153del	XP_011520728.1:n.*149_*153del
XM_011522427.1:c.*149_*153del	XP_011520729.1:n.*149_*153del
XR_932805.1:n.3059_3063del
XM_011522424.3:c.*149_*153del	XP_011520726.1:n.*149_*153del
XM_017023043.2:c.*149_*153del	XP_016878532.1:n.*149_*153del
NM_005236.3:c.*149_*153del MANE Select	NP_005227.1:n.*149_*153del