Canonical Allele Identifier: CA493690055

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14041871T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948014T>G , CM000678.2:g.13948014T>G	GRCh38
NC_000016.9:g.14041871T>G , CM000678.1:g.14041871T>G	GRCh37
NC_000016.8:g.13949372T>G	NCBI36
NG_011442.1:g.32858T>G , LRG_463:g.32858T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2556T>G	ENSP00000507912.1:p.Pro852=
ENST00000683962.1:c.*2112T>G	ENSP00000506854.1:n.*2112T>G
ENST00000311895.8:c.2418T>G MANE Select	ENSP00000310520.7:p.Pro806=
ENST00000311895.7:c.2418T>G	ENSP00000310520.7:p.Pro806=
ENST00000389138.7:n.1695T>G
NM_005236.2:c.2418T>G , LRG_463t1:c.2418T>G	NP_005227.1:p.Pro806=
XM_011522424.1:c.2556T>G	XP_011520726.1:p.Pro852=
XM_011522425.1:c.1875T>G	XP_011520727.1:p.Pro625=
XM_011522426.1:c.1629T>G	XP_011520728.1:p.Pro543=
XM_011522427.1:c.1068T>G	XP_011520729.1:p.Pro356=
XR_932805.1:n.2577T>G
XM_011522424.3:c.2556T>G	XP_011520726.1:p.Pro852=
XM_017023043.2:c.1629T>G	XP_016878532.1:p.Pro543=
NM_005236.3:c.2418T>G MANE Select	NP_005227.1:p.Pro806=