Canonical Allele Identifier: CA493444473

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14042084A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948227A>C , CM000678.2:g.13948227A>C	GRCh38
NC_000016.9:g.14042084A>C , CM000678.1:g.14042084A>C	GRCh37
NC_000016.8:g.13949585A>C	NCBI36
NG_011442.1:g.33071A>C , LRG_463:g.33071A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2769A>C	ENSP00000507912.1:p.Ala923=
ENST00000683962.1:c.*2325A>C	ENSP00000506854.1:n.*2325A>C
ENST00000311895.8:c.2631A>C MANE Select	ENSP00000310520.7:p.Ala877=
ENST00000311895.7:c.2631A>C	ENSP00000310520.7:p.Ala877=
ENST00000389138.7:n.1908A>C
NM_005236.2:c.2631A>C , LRG_463t1:c.2631A>C	NP_005227.1:p.Ala877=
XM_011522424.1:c.2769A>C	XP_011520726.1:p.Ala923=
XM_011522425.1:c.2088A>C	XP_011520727.1:p.Ala696=
XM_011522426.1:c.1842A>C	XP_011520728.1:p.Ala614=
XM_011522427.1:c.1281A>C	XP_011520729.1:p.Ala427=
XR_932805.1:n.2790A>C
XM_011522424.3:c.2769A>C	XP_011520726.1:p.Ala923=
XM_017023043.2:c.1842A>C	XP_016878532.1:p.Ala614=
NM_005236.3:c.2631A>C MANE Select	NP_005227.1:p.Ala877=