Canonical Allele Identifier: CA394812334

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029464G>C (hg19) ; chr16:g.13935607G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935607G>C , CM000678.2:g.13935607G>C	GRCh38
NC_000016.9:g.14029464G>C , CM000678.1:g.14029464G>C	GRCh37
NC_000016.8:g.13936965G>C	NCBI36
NG_011442.1:g.20451G>C , LRG_463:g.20451G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1753G>C
ENST00000682617.1:c.1813G>C	ENSP00000507912.1:p.Gly605Arg
ENST00000682826.1:c.*989G>C	ENSP00000507274.1:n.*989G>C
ENST00000682909.1:n.3715G>C
ENST00000683277.1:n.3320G>C
ENST00000683407.1:n.1683G>C
ENST00000683962.1:c.*1369G>C	ENSP00000506854.1:n.*1369G>C
ENST00000311895.8:c.1675G>C MANE Select	ENSP00000310520.7:p.Gly559Arg
ENST00000311895.7:c.1675G>C	ENSP00000310520.7:p.Gly559Arg
ENST00000389138.7:n.952G>C
NM_005236.2:c.1675G>C , LRG_463t1:c.1675G>C	NP_005227.1:p.Gly559Arg
XM_011522424.1:c.1813G>C	XP_011520726.1:p.Gly605Arg
XM_011522425.1:c.1132G>C	XP_011520727.1:p.Gly378Arg
XM_011522426.1:c.886G>C	XP_011520728.1:p.Gly296Arg
XM_011522427.1:c.325G>C	XP_011520729.1:p.Gly109Arg
XR_932805.1:n.1834G>C
XM_011522424.3:c.1813G>C	XP_011520726.1:p.Gly605Arg
XM_017023043.2:c.886G>C	XP_016878532.1:p.Gly296Arg
NM_005236.3:c.1675G>C MANE Select	NP_005227.1:p.Gly559Arg