Canonical Allele Identifier: CA394811437

Gene: ERCC4

Linked Data

• dbSNP Id: rs200617058
• gnomAD v2: 16-14029320-G-T
• gnomAD v4: 16-13935463-G-T
• MyVariant Identifiers: chr16:g.14029320G>T (hg19) ; chr16:g.13935463G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935463G>T , CM000678.2:g.13935463G>T	GRCh38
NC_000016.9:g.14029320G>T , CM000678.1:g.14029320G>T	GRCh37
NC_000016.8:g.13936821G>T	NCBI36
NG_011442.1:g.20307G>T , LRG_463:g.20307G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1609G>T
ENST00000682617.1:c.1669G>T	ENSP00000507912.1:p.Glu557Ter
ENST00000682826.1:c.*845G>T	ENSP00000507274.1:n.*845G>T
ENST00000682909.1:n.3571G>T
ENST00000683277.1:n.3176G>T
ENST00000683407.1:n.1539G>T
ENST00000683962.1:c.*1225G>T	ENSP00000506854.1:n.*1225G>T
ENST00000311895.8:c.1531G>T MANE Select	ENSP00000310520.7:p.Glu511Ter
ENST00000311895.7:c.1531G>T	ENSP00000310520.7:p.Glu511Ter
ENST00000389138.7:n.808G>T
NM_005236.2:c.1531G>T , LRG_463t1:c.1531G>T	NP_005227.1:p.Glu511Ter
XM_011522424.1:c.1669G>T	XP_011520726.1:p.Glu557Ter
XM_011522425.1:c.988G>T	XP_011520727.1:p.Glu330Ter
XM_011522426.1:c.742G>T	XP_011520728.1:p.Glu248Ter
XM_011522427.1:c.181G>T	XP_011520729.1:p.Glu61Ter
XR_932805.1:n.1690G>T
XM_011522424.3:c.1669G>T	XP_011520726.1:p.Glu557Ter
XM_017023043.2:c.742G>T	XP_016878532.1:p.Glu248Ter
NM_005236.3:c.1531G>T MANE Select	NP_005227.1:p.Glu511Ter