Canonical Allele Identifier: CA394824464

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948160T>A , CM000678.2:g.13948160T>A	GRCh38
NC_000016.9:g.14042017T>A , CM000678.1:g.14042017T>A	GRCh37
NC_000016.8:g.13949518T>A	NCBI36
NG_011442.1:g.33004T>A , LRG_463:g.33004T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005236.3:c.2564T>A MANE Select	NP_005227.1:p.Met855Lys
ENST00000311895.8:c.2564T>A MANE Select	ENSP00000310520.7:p.Met855Lys
NM_005236.2:c.2564T>A , LRG_463t1:c.2564T>A	NP_005227.1:p.Met855Lys
ENST00000311895.7:c.2564T>A	ENSP00000310520.7:p.Met855Lys
ENST00000389138.7:n.1841T>A
ENST00000682617.1:c.2702T>A	ENSP00000507912.1:p.Met901Lys
ENST00000683962.1:c.*2258T>A	ENSP00000506854.1:n.*2258T>A
XM_011522424.1:c.2702T>A	XP_011520726.1:p.Met901Lys
XM_011522424.3:c.2702T>A	XP_011520726.1:p.Met901Lys
XM_011522425.1:c.2021T>A	XP_011520727.1:p.Met674Lys
XM_011522426.1:c.1775T>A	XP_011520728.1:p.Met592Lys
XM_011522427.1:c.1214T>A	XP_011520729.1:p.Met405Lys
XM_017023043.2:c.1775T>A	XP_016878532.1:p.Met592Lys
XR_932805.1:n.2723T>A