Canonical Allele Identifier: CA376723376
Community Standard Title: NM_000124.4(ERCC6):c.2286+1G>A
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49478353C>T , CM000672.2:g.49478353C>T GRCh38
NC_000010.10:g.50686399C>T , CM000672.1:g.50686399C>T GRCh37
NC_000010.9:g.50356405C>T NCBI36
NG_009442.1:g.65749G>A , LRG_465:g.65749G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000124.4:c.2286+1G>A MANE Select NP_000115.1:n.2286+1G>A
ENST00000355832.10:c.2286+1G>A MANE Select ENSP00000348089.5:n.2286+1G>A
NM_000124.3:c.2286+1G>A NP_000115.1:n.2286+1G>A
NM_001346440.1:c.2286+1G>A NP_001333369.1:n.2286+1G>A
NM_001346440.2:c.2286+1G>A NP_001333369.1:n.2286+1G>A
ENST00000355832.9:c.2286+1G>A ENSP00000348089.5:n.2286+1G>A
ENST00000623073.3:c.*678+1G>A ENSP00000485650.1:n.*678+1G>A
ENST00000623115.3:c.396+1G>A ENSP00000485321.1:n.396+1G>A
ENST00000681632.1:n.2364+1G>A
ENST00000681659.1:c.2127+1G>A ENSP00000505631.1:n.2127+1G>A