Canonical Allele Identifier: CA493689769

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029328A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935471A>C , CM000678.2:g.13935471A>C	GRCh38
NC_000016.9:g.14029328A>C , CM000678.1:g.14029328A>C	GRCh37
NC_000016.8:g.13936829A>C	NCBI36
NG_011442.1:g.20315A>C , LRG_463:g.20315A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1617A>C
ENST00000682617.1:c.1677A>C	ENSP00000507912.1:p.Gly559=
ENST00000682826.1:c.*853A>C	ENSP00000507274.1:n.*853A>C
ENST00000682909.1:n.3579A>C
ENST00000683277.1:n.3184A>C
ENST00000683407.1:n.1547A>C
ENST00000683962.1:c.*1233A>C	ENSP00000506854.1:n.*1233A>C
ENST00000311895.8:c.1539A>C MANE Select	ENSP00000310520.7:p.Gly513=
ENST00000311895.7:c.1539A>C	ENSP00000310520.7:p.Gly513=
ENST00000389138.7:n.816A>C
NM_005236.2:c.1539A>C , LRG_463t1:c.1539A>C	NP_005227.1:p.Gly513=
XM_011522424.1:c.1677A>C	XP_011520726.1:p.Gly559=
XM_011522425.1:c.996A>C	XP_011520727.1:p.Gly332=
XM_011522426.1:c.750A>C	XP_011520728.1:p.Gly250=
XM_011522427.1:c.189A>C	XP_011520729.1:p.Gly63=
XR_932805.1:n.1698A>C
XM_011522424.3:c.1677A>C	XP_011520726.1:p.Gly559=
XM_017023043.2:c.750A>C	XP_016878532.1:p.Gly250=
NM_005236.3:c.1539A>C MANE Select	NP_005227.1:p.Gly513=