Canonical Allele Identifier: CA394812084

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029427C>G (hg19) ; chr16:g.13935570C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935570C>G , CM000678.2:g.13935570C>G	GRCh38
NC_000016.9:g.14029427C>G , CM000678.1:g.14029427C>G	GRCh37
NC_000016.8:g.13936928C>G	NCBI36
NG_011442.1:g.20414C>G , LRG_463:g.20414C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1716C>G
ENST00000682617.1:c.1776C>G	ENSP00000507912.1:p.Ile592Met
ENST00000682826.1:c.*952C>G	ENSP00000507274.1:n.*952C>G
ENST00000682909.1:n.3678C>G
ENST00000683277.1:n.3283C>G
ENST00000683407.1:n.1646C>G
ENST00000683962.1:c.*1332C>G	ENSP00000506854.1:n.*1332C>G
ENST00000311895.8:c.1638C>G MANE Select	ENSP00000310520.7:p.Ile546Met
ENST00000311895.7:c.1638C>G	ENSP00000310520.7:p.Ile546Met
ENST00000389138.7:n.915C>G
NM_005236.2:c.1638C>G , LRG_463t1:c.1638C>G	NP_005227.1:p.Ile546Met
XM_011522424.1:c.1776C>G	XP_011520726.1:p.Ile592Met
XM_011522425.1:c.1095C>G	XP_011520727.1:p.Ile365Met
XM_011522426.1:c.849C>G	XP_011520728.1:p.Ile283Met
XM_011522427.1:c.288C>G	XP_011520729.1:p.Ile96Met
XR_932805.1:n.1797C>G
XM_011522424.3:c.1776C>G	XP_011520726.1:p.Ile592Met
XM_017023043.2:c.849C>G	XP_016878532.1:p.Ile283Met
NM_005236.3:c.1638C>G MANE Select	NP_005227.1:p.Ile546Met