Canonical Allele Identifier: CA376726530

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50701231A>T (hg19) ; chr10:g.49493185A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49493185A>T , CM000672.2:g.49493185A>T	GRCh38
NC_000010.10:g.50701231A>T , CM000672.1:g.50701231A>T	GRCh37
NC_000010.9:g.50371237A>T	NCBI36
NG_009442.1:g.50917T>A , LRG_465:g.50917T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.1753T>A MANE Select	ENSP00000348089.5:p.Phe585Ile
ENST00000681632.1:n.1831T>A
ENST00000681659.1:c.1594T>A	ENSP00000505631.1:p.Phe532Ile
ENST00000355832.9:c.1753T>A	ENSP00000348089.5:p.Phe585Ile
ENST00000475116.1:n.275+7353T>A
ENST00000623073.3:c.154T>A	ENSP00000485650.1:p.Phe52Ile
ENST00000623115.3:c.-70+7353T>A	ENSP00000485321.1:n.-70+7353T>A
ENST00000623318.1:c.154T>A	ENSP00000485423.1:p.Phe52Ile
NM_000124.3:c.1753T>A	NP_000115.1:p.Phe585Ile
NM_001346440.1:c.1753T>A	NP_001333369.1:p.Phe585Ile
NM_000124.4:c.1753T>A MANE Select	NP_000115.1:p.Phe585Ile
NM_001346440.2:c.1753T>A	NP_001333369.1:p.Phe585Ile