Canonical Allele Identifier: CA394812701

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029565A>C (hg19) ; chr16:g.13935708A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935708A>C , CM000678.2:g.13935708A>C	GRCh38
NC_000016.9:g.14029565A>C , CM000678.1:g.14029565A>C	GRCh37
NC_000016.8:g.13937066A>C	NCBI36
NG_011442.1:g.20552A>C , LRG_463:g.20552A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1854A>C
ENST00000682617.1:c.1914A>C	ENSP00000507912.1:p.Glu638Asp
ENST00000682826.1:c.*1090A>C	ENSP00000507274.1:n.*1090A>C
ENST00000682909.1:n.3816A>C
ENST00000683277.1:n.3421A>C
ENST00000683407.1:n.1784A>C
ENST00000683962.1:c.*1470A>C	ENSP00000506854.1:n.*1470A>C
ENST00000311895.8:c.1776A>C MANE Select	ENSP00000310520.7:p.Glu592Asp
ENST00000311895.7:c.1776A>C	ENSP00000310520.7:p.Glu592Asp
ENST00000389138.7:n.1053A>C
NM_005236.2:c.1776A>C , LRG_463t1:c.1776A>C	NP_005227.1:p.Glu592Asp
XM_011522424.1:c.1914A>C	XP_011520726.1:p.Glu638Asp
XM_011522425.1:c.1233A>C	XP_011520727.1:p.Glu411Asp
XM_011522426.1:c.987A>C	XP_011520728.1:p.Glu329Asp
XM_011522427.1:c.426A>C	XP_011520729.1:p.Glu142Asp
XR_932805.1:n.1935A>C
XM_011522424.3:c.1914A>C	XP_011520726.1:p.Glu638Asp
XM_017023043.2:c.987A>C	XP_016878532.1:p.Glu329Asp
NM_005236.3:c.1776A>C MANE Select	NP_005227.1:p.Glu592Asp