Canonical Allele Identifier: CA152774

Linked Data

ClinVar Variation Id: 129013
dbSNP Id: rs2228528

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49524234C>T , CM000672.2:g.49524234C>T GRCh38
NC_000010.10:g.50732280C>T , CM000672.1:g.50732280C>T GRCh37
NC_000010.9:g.50402286C>T NCBI36
NG_009442.1:g.19868G>A , LRG_465:g.19868G>A
NG_033155.1:g.5048G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.1196G>A (ERCC6) MANE Select ENSP00000348089.5:p.Gly399Asp
ENST00000447839.7:c.1196G>A (ERCC6) MANE Plus Clinical ENSP00000387966.2:p.Gly399Asp
ENST00000679596.1:c.*825G>A (ERCC6) ENSP00000504862.1:n.*825G>A
ENST00000679811.1:n.1279G>A (ERCC6)
ENST00000680107.1:c.652+4183G>A (ERCC6) ENSP00000505909.1:n.652+4183G>A
ENST00000680233.1:n.1289G>A (ERCC6)
ENST00000681632.1:n.1274G>A (ERCC6)
ENST00000681659.1:c.1196G>A (ERCC6) ENSP00000505631.1:p.Gly399Asp
ENST00000355832.9:c.1196G>A (ERCC6) ENSP00000348089.5:p.Gly399Asp
ENST00000447839.6:c.1196G>A ENSP00000387966.2:p.Gly399Asp
ENST00000515869.1:c.1196G>A ENSP00000423550.1:p.Gly399Asp
NM_000124.3:c.1196G>A (ERCC6) NP_000115.1:p.Gly399Asp
NM_001277058.1:c.1196G>A NP_001263987.1:p.Gly399Asp
NM_001277059.1:c.1196G>A NP_001263988.1:p.Gly399Asp
NM_170753.3:c.-209G>A (PGBD3) NP_736609.2:n.-209G>A
NM_001346440.1:c.1196G>A (ERCC6) NP_001333369.1:p.Gly399Asp
NM_000124.4:c.1196G>A (ERCC6) MANE Select NP_000115.1:p.Gly399Asp
NM_001277058.2:c.1196G>A (ERCC6) MANE Plus Clinical NP_001263987.1:p.Gly399Asp
NM_001277059.2:c.1196G>A (ERCC6) NP_001263988.1:p.Gly399Asp
NM_001346440.2:c.1196G>A (ERCC6) NP_001333369.1:p.Gly399Asp