Canonical Allele Identifier: CA493444474
Gene: ERCC4 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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