Canonical Allele Identifier: CA493444503

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14042126T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948269T>C , CM000678.2:g.13948269T>C	GRCh38
NC_000016.9:g.14042126T>C , CM000678.1:g.14042126T>C	GRCh37
NC_000016.8:g.13949627T>C	NCBI36
NG_011442.1:g.33113T>C , LRG_463:g.33113T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2811T>C	ENSP00000507912.1:p.Ala937=
ENST00000683962.1:c.*2367T>C	ENSP00000506854.1:n.*2367T>C
ENST00000311895.8:c.2673T>C MANE Select	ENSP00000310520.7:p.Ala891=
ENST00000311895.7:c.2673T>C	ENSP00000310520.7:p.Ala891=
ENST00000389138.7:n.1950T>C
NM_005236.2:c.2673T>C , LRG_463t1:c.2673T>C	NP_005227.1:p.Ala891=
XM_011522424.1:c.2811T>C	XP_011520726.1:p.Ala937=
XM_011522425.1:c.2130T>C	XP_011520727.1:p.Ala710=
XM_011522426.1:c.1884T>C	XP_011520728.1:p.Ala628=
XM_011522427.1:c.1323T>C	XP_011520729.1:p.Ala441=
XR_932805.1:n.2832T>C
XM_011522424.3:c.2811T>C	XP_011520726.1:p.Ala937=
XM_017023043.2:c.1884T>C	XP_016878532.1:p.Ala628=
NM_005236.3:c.2673T>C MANE Select	NP_005227.1:p.Ala891=