Canonical Allele Identifier: CA2843129372
Gene: ERCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49472565T>C , CM000672.2:g.49472565T>C GRCh38
NC_000010.10:g.50680611T>C , CM000672.1:g.50680611T>C GRCh37
NC_000010.9:g.50350617T>C NCBI36
NG_009442.1:g.71537A>G , LRG_465:g.71537A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355832.10:c.2830-95A>G MANE Select ENSP00000348089.5:n.2830-95A>G
ENST00000681632.1:n.4138A>G
ENST00000681659.1:c.2671-95A>G ENSP00000505631.1:n.2671-95A>G
ENST00000355832.9:c.2830-95A>G ENSP00000348089.5:n.2830-95A>G
ENST00000623073.3:c.*1126-95A>G ENSP00000485650.1:n.*1126-95A>G
ENST00000623115.3:c.940-95A>G ENSP00000485321.1:n.940-95A>G
ENST00000624341.3:c.662-95A>G
NM_000124.3:c.2830-95A>G NP_000115.1:n.2830-95A>G
XR_945953.1:n.690-138T>C
NM_001346440.1:c.2830-95A>G NP_001333369.1:n.2830-95A>G
NM_000124.4:c.2830-95A>G MANE Select NP_000115.1:n.2830-95A>G
NM_001346440.2:c.2830-95A>G NP_001333369.1:n.2830-95A>G