Canonical Allele Identifier: CA394824422
Gene: ERCC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13948142A>C , CM000678.2:g.13948142A>C GRCh38
NC_000016.9:g.14041999A>C , CM000678.1:g.14041999A>C GRCh37
NC_000016.8:g.13949500A>C NCBI36
NG_011442.1:g.32986A>C , LRG_463:g.32986A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2684A>C ENSP00000507912.1:p.Gln895Pro
ENST00000683962.1:c.*2240A>C ENSP00000506854.1:n.*2240A>C
ENST00000311895.8:c.2546A>C MANE Select ENSP00000310520.7:p.Gln849Pro
ENST00000311895.7:c.2546A>C ENSP00000310520.7:p.Gln849Pro
ENST00000389138.7:n.1823A>C
NM_005236.2:c.2546A>C , LRG_463t1:c.2546A>C NP_005227.1:p.Gln849Pro
XM_011522424.1:c.2684A>C XP_011520726.1:p.Gln895Pro
XM_011522425.1:c.2003A>C XP_011520727.1:p.Gln668Pro
XM_011522426.1:c.1757A>C XP_011520728.1:p.Gln586Pro
XM_011522427.1:c.1196A>C XP_011520729.1:p.Gln399Pro
XR_932805.1:n.2705A>C
XM_011522424.3:c.2684A>C XP_011520726.1:p.Gln895Pro
XM_017023043.2:c.1757A>C XP_016878532.1:p.Gln586Pro
NM_005236.3:c.2546A>C MANE Select NP_005227.1:p.Gln849Pro