Canonical Allele Identifier: CA394811899

Gene: ERCC4

Linked Data

• gnomAD v4: 16-13935541-A-T
• MyVariant Identifiers: chr16:g.14029398A>T (hg19) ; chr16:g.13935541A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935541A>T , CM000678.2:g.13935541A>T	GRCh38
NC_000016.9:g.14029398A>T , CM000678.1:g.14029398A>T	GRCh37
NC_000016.8:g.13936899A>T	NCBI36
NG_011442.1:g.20385A>T , LRG_463:g.20385A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1687A>T
ENST00000682617.1:c.1747A>T	ENSP00000507912.1:p.Asn583Tyr
ENST00000682826.1:c.*923A>T	ENSP00000507274.1:n.*923A>T
ENST00000682909.1:n.3649A>T
ENST00000683277.1:n.3254A>T
ENST00000683407.1:n.1617A>T
ENST00000683962.1:c.*1303A>T	ENSP00000506854.1:n.*1303A>T
ENST00000311895.8:c.1609A>T MANE Select	ENSP00000310520.7:p.Asn537Tyr
ENST00000311895.7:c.1609A>T	ENSP00000310520.7:p.Asn537Tyr
ENST00000389138.7:n.886A>T
NM_005236.2:c.1609A>T , LRG_463t1:c.1609A>T	NP_005227.1:p.Asn537Tyr
XM_011522424.1:c.1747A>T	XP_011520726.1:p.Asn583Tyr
XM_011522425.1:c.1066A>T	XP_011520727.1:p.Asn356Tyr
XM_011522426.1:c.820A>T	XP_011520728.1:p.Asn274Tyr
XM_011522427.1:c.259A>T	XP_011520729.1:p.Asn87Tyr
XR_932805.1:n.1768A>T
XM_011522424.3:c.1747A>T	XP_011520726.1:p.Asn583Tyr
XM_017023043.2:c.820A>T	XP_016878532.1:p.Asn274Tyr
NM_005236.3:c.1609A>T MANE Select	NP_005227.1:p.Asn537Tyr