Canonical Allele Identifier: CA394823990

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14041920C>A (hg19) ; chr16:g.13948063C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948063C>A , CM000678.2:g.13948063C>A	GRCh38
NC_000016.9:g.14041920C>A , CM000678.1:g.14041920C>A	GRCh37
NC_000016.8:g.13949421C>A	NCBI36
NG_011442.1:g.32907C>A , LRG_463:g.32907C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2605C>A	ENSP00000507912.1:p.Pro869Thr
ENST00000683962.1:c.*2161C>A	ENSP00000506854.1:n.*2161C>A
ENST00000311895.8:c.2467C>A MANE Select	ENSP00000310520.7:p.Pro823Thr
ENST00000311895.7:c.2467C>A	ENSP00000310520.7:p.Pro823Thr
ENST00000389138.7:n.1744C>A
NM_005236.2:c.2467C>A , LRG_463t1:c.2467C>A	NP_005227.1:p.Pro823Thr
XM_011522424.1:c.2605C>A	XP_011520726.1:p.Pro869Thr
XM_011522425.1:c.1924C>A	XP_011520727.1:p.Pro642Thr
XM_011522426.1:c.1678C>A	XP_011520728.1:p.Pro560Thr
XM_011522427.1:c.1117C>A	XP_011520729.1:p.Pro373Thr
XR_932805.1:n.2626C>A
XM_011522424.3:c.2605C>A	XP_011520726.1:p.Pro869Thr
XM_017023043.2:c.1678C>A	XP_016878532.1:p.Pro560Thr
NM_005236.3:c.2467C>A MANE Select	NP_005227.1:p.Pro823Thr