Canonical Allele Identifier: CA493690071

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14041901G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948044G>T , CM000678.2:g.13948044G>T	GRCh38
NC_000016.9:g.14041901G>T , CM000678.1:g.14041901G>T	GRCh37
NC_000016.8:g.13949402G>T	NCBI36
NG_011442.1:g.32888G>T , LRG_463:g.32888G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2586G>T	ENSP00000507912.1:p.Leu862=
ENST00000683962.1:c.*2142G>T	ENSP00000506854.1:n.*2142G>T
ENST00000311895.8:c.2448G>T MANE Select	ENSP00000310520.7:p.Leu816=
ENST00000311895.7:c.2448G>T	ENSP00000310520.7:p.Leu816=
ENST00000389138.7:n.1725G>T
NM_005236.2:c.2448G>T , LRG_463t1:c.2448G>T	NP_005227.1:p.Leu816=
XM_011522424.1:c.2586G>T	XP_011520726.1:p.Leu862=
XM_011522425.1:c.1905G>T	XP_011520727.1:p.Leu635=
XM_011522426.1:c.1659G>T	XP_011520728.1:p.Leu553=
XM_011522427.1:c.1098G>T	XP_011520729.1:p.Leu366=
XR_932805.1:n.2607G>T
XM_011522424.3:c.2586G>T	XP_011520726.1:p.Leu862=
XM_017023043.2:c.1659G>T	XP_016878532.1:p.Leu553=
NM_005236.3:c.2448G>T MANE Select	NP_005227.1:p.Leu816=