Canonical Allele Identifier: CA394823928

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14041911A>C (hg19) ; chr16:g.13948054A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948054A>C , CM000678.2:g.13948054A>C	GRCh38
NC_000016.9:g.14041911A>C , CM000678.1:g.14041911A>C	GRCh37
NC_000016.8:g.13949412A>C	NCBI36
NG_011442.1:g.32898A>C , LRG_463:g.32898A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2596A>C	ENSP00000507912.1:p.Lys866Gln
ENST00000683962.1:c.*2152A>C	ENSP00000506854.1:n.*2152A>C
ENST00000311895.8:c.2458A>C MANE Select	ENSP00000310520.7:p.Lys820Gln
ENST00000311895.7:c.2458A>C	ENSP00000310520.7:p.Lys820Gln
ENST00000389138.7:n.1735A>C
NM_005236.2:c.2458A>C , LRG_463t1:c.2458A>C	NP_005227.1:p.Lys820Gln
XM_011522424.1:c.2596A>C	XP_011520726.1:p.Lys866Gln
XM_011522425.1:c.1915A>C	XP_011520727.1:p.Lys639Gln
XM_011522426.1:c.1669A>C	XP_011520728.1:p.Lys557Gln
XM_011522427.1:c.1108A>C	XP_011520729.1:p.Lys370Gln
XR_932805.1:n.2617A>C
XM_011522424.3:c.2596A>C	XP_011520726.1:p.Lys866Gln
XM_017023043.2:c.1669A>C	XP_016878532.1:p.Lys557Gln
NM_005236.3:c.2458A>C MANE Select	NP_005227.1:p.Lys820Gln