Canonical Allele Identifier: CA394812725

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029570A>G (hg19) ; chr16:g.13935713A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935713A>G , CM000678.2:g.13935713A>G	GRCh38
NC_000016.9:g.14029570A>G , CM000678.1:g.14029570A>G	GRCh37
NC_000016.8:g.13937071A>G	NCBI36
NG_011442.1:g.20557A>G , LRG_463:g.20557A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1859A>G
ENST00000682617.1:c.1919A>G	ENSP00000507912.1:p.Tyr640Cys
ENST00000682826.1:c.*1095A>G	ENSP00000507274.1:n.*1095A>G
ENST00000682909.1:n.3821A>G
ENST00000683277.1:n.3426A>G
ENST00000683407.1:n.1789A>G
ENST00000683962.1:c.*1475A>G	ENSP00000506854.1:n.*1475A>G
ENST00000311895.8:c.1781A>G MANE Select	ENSP00000310520.7:p.Tyr594Cys
ENST00000311895.7:c.1781A>G	ENSP00000310520.7:p.Tyr594Cys
ENST00000389138.7:n.1058A>G
NM_005236.2:c.1781A>G , LRG_463t1:c.1781A>G	NP_005227.1:p.Tyr594Cys
XM_011522424.1:c.1919A>G	XP_011520726.1:p.Tyr640Cys
XM_011522425.1:c.1238A>G	XP_011520727.1:p.Tyr413Cys
XM_011522426.1:c.992A>G	XP_011520728.1:p.Tyr331Cys
XM_011522427.1:c.431A>G	XP_011520729.1:p.Tyr144Cys
XR_932805.1:n.1940A>G
XM_011522424.3:c.1919A>G	XP_011520726.1:p.Tyr640Cys
XM_017023043.2:c.992A>G	XP_016878532.1:p.Tyr331Cys
NM_005236.3:c.1781A>G MANE Select	NP_005227.1:p.Tyr594Cys