Canonical Allele Identifier: CA493689518

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029481T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935624T>C , CM000678.2:g.13935624T>C	GRCh38
NC_000016.9:g.14029481T>C , CM000678.1:g.14029481T>C	GRCh37
NC_000016.8:g.13936982T>C	NCBI36
NG_011442.1:g.20468T>C , LRG_463:g.20468T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1770T>C
ENST00000682617.1:c.1830T>C	ENSP00000507912.1:p.Tyr610=
ENST00000682826.1:c.*1006T>C	ENSP00000507274.1:n.*1006T>C
ENST00000682909.1:n.3732T>C
ENST00000683277.1:n.3337T>C
ENST00000683407.1:n.1700T>C
ENST00000683962.1:c.*1386T>C	ENSP00000506854.1:n.*1386T>C
ENST00000311895.8:c.1692T>C MANE Select	ENSP00000310520.7:p.Tyr564=
ENST00000311895.7:c.1692T>C	ENSP00000310520.7:p.Tyr564=
ENST00000389138.7:n.969T>C
NM_005236.2:c.1692T>C , LRG_463t1:c.1692T>C	NP_005227.1:p.Tyr564=
XM_011522424.1:c.1830T>C	XP_011520726.1:p.Tyr610=
XM_011522425.1:c.1149T>C	XP_011520727.1:p.Tyr383=
XM_011522426.1:c.903T>C	XP_011520728.1:p.Tyr301=
XM_011522427.1:c.342T>C	XP_011520729.1:p.Tyr114=
XR_932805.1:n.1851T>C
XM_011522424.3:c.1830T>C	XP_011520726.1:p.Tyr610=
XM_017023043.2:c.903T>C	XP_016878532.1:p.Tyr301=
NM_005236.3:c.1692T>C MANE Select	NP_005227.1:p.Tyr564=