Canonical Allele Identifier: CA621178933

Gene: ERCC4

Linked Data

• dbSNP Id: rs1163110186
• gnomAD v2: 16-14042287-G-T
• gnomAD v3: 16-13948430-G-T
• gnomAD v4: 16-13948430-G-T
• MyVariant Identifiers: chr16:g.14042287G>T (hg19) ; chr16:g.13948430G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948430G>T , CM000678.2:g.13948430G>T	GRCh38
NC_000016.9:g.14042287G>T , CM000678.1:g.14042287G>T	GRCh37
NC_000016.8:g.13949788G>T	NCBI36
NG_011442.1:g.33274G>T , LRG_463:g.33274G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.*83G>T	ENSP00000507912.1:n.*83G>T
ENST00000683962.1:c.*2528G>T	ENSP00000506854.1:n.*2528G>T
ENST00000311895.8:c.*83G>T MANE Select	ENSP00000310520.7:n.*83G>T
ENST00000311895.7:c.*83G>T	ENSP00000310520.7:n.*83G>T
NM_005236.2:c.*83G>T , LRG_463t1:c.*83G>T	NP_005227.1:n.*83G>T
XM_011522424.1:c.*83G>T	XP_011520726.1:n.*83G>T
XM_011522425.1:c.*83G>T	XP_011520727.1:n.*83G>T
XM_011522426.1:c.*83G>T	XP_011520728.1:n.*83G>T
XM_011522427.1:c.*83G>T	XP_011520729.1:n.*83G>T
XR_932805.1:n.2993G>T
XM_011522424.3:c.*83G>T	XP_011520726.1:n.*83G>T
XM_017023043.2:c.*83G>T	XP_016878532.1:n.*83G>T
NM_005236.3:c.*83G>T MANE Select	NP_005227.1:n.*83G>T