Canonical Allele Identifier: CA2731935189
Gene: ERCC4 HGNC NCBI

Linked Data

dbSNP Id: rs2032568451

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948407T>G , CM000678.2:g.13948407T>G GRCh38
NC_000016.9:g.14042264T>G , CM000678.1:g.14042264T>G GRCh37
NC_000016.8:g.13949765T>G NCBI36
NG_011442.1:g.33251T>G , LRG_463:g.33251T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682617.1:c.*60T>G ENSP00000507912.1:n.*60T>G
ENST00000683962.1:c.*2505T>G ENSP00000506854.1:n.*2505T>G
ENST00000311895.8:c.*60T>G MANE Select ENSP00000310520.7:n.*60T>G
ENST00000311895.7:c.*60T>G ENSP00000310520.7:n.*60T>G
ENST00000389138.7:n.2088T>G
NM_005236.2:c.*60T>G , LRG_463t1:c.*60T>G NP_005227.1:n.*60T>G
XM_011522424.1:c.*60T>G XP_011520726.1:n.*60T>G
XM_011522425.1:c.*60T>G XP_011520727.1:n.*60T>G
XM_011522426.1:c.*60T>G XP_011520728.1:n.*60T>G
XM_011522427.1:c.*60T>G XP_011520729.1:n.*60T>G
XR_932805.1:n.2970T>G
XM_011522424.3:c.*60T>G XP_011520726.1:n.*60T>G
XM_017023043.2:c.*60T>G XP_016878532.1:n.*60T>G
NM_005236.3:c.*60T>G MANE Select NP_005227.1:n.*60T>G