Canonical Allele Identifier: CA394811821

Gene: ERCC4

Linked Data

• MyVariant Identifiers: chr16:g.14029389T>C (hg19) ; chr16:g.13935532T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935532T>C , CM000678.2:g.13935532T>C	GRCh38
NC_000016.9:g.14029389T>C , CM000678.1:g.14029389T>C	GRCh37
NC_000016.8:g.13936890T>C	NCBI36
NG_011442.1:g.20376T>C , LRG_463:g.20376T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1678T>C
ENST00000682617.1:c.1738T>C	ENSP00000507912.1:p.Phe580Leu
ENST00000682826.1:c.*914T>C	ENSP00000507274.1:n.*914T>C
ENST00000682909.1:n.3640T>C
ENST00000683277.1:n.3245T>C
ENST00000683407.1:n.1608T>C
ENST00000683962.1:c.*1294T>C	ENSP00000506854.1:n.*1294T>C
ENST00000311895.8:c.1600T>C MANE Select	ENSP00000310520.7:p.Phe534Leu
ENST00000311895.7:c.1600T>C	ENSP00000310520.7:p.Phe534Leu
ENST00000389138.7:n.877T>C
NM_005236.2:c.1600T>C , LRG_463t1:c.1600T>C	NP_005227.1:p.Phe534Leu
XM_011522424.1:c.1738T>C	XP_011520726.1:p.Phe580Leu
XM_011522425.1:c.1057T>C	XP_011520727.1:p.Phe353Leu
XM_011522426.1:c.811T>C	XP_011520728.1:p.Phe271Leu
XM_011522427.1:c.250T>C	XP_011520729.1:p.Phe84Leu
XR_932805.1:n.1759T>C
XM_011522424.3:c.1738T>C	XP_011520726.1:p.Phe580Leu
XM_017023043.2:c.811T>C	XP_016878532.1:p.Phe271Leu
NM_005236.3:c.1600T>C MANE Select	NP_005227.1:p.Phe534Leu