Canonical Allele Identifier: CA376729190

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50708723T>A (hg19) ; chr10:g.49500677T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49500677T>A , CM000672.2:g.49500677T>A	GRCh38
NC_000010.10:g.50708723T>A , CM000672.1:g.50708723T>A	GRCh37
NC_000010.9:g.50378729T>A	NCBI36
NG_009442.1:g.43425A>T , LRG_465:g.43425A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.1546A>T MANE Select	ENSP00000348089.5:p.Arg516Trp
ENST00000681632.1:n.1624A>T
ENST00000681659.1:c.1526+5207A>T	ENSP00000505631.1:n.1526+5207A>T
ENST00000355832.9:c.1546A>T	ENSP00000348089.5:p.Arg516Trp
ENST00000475116.1:n.136A>T
ENST00000623073.3:c.-54A>T	ENSP00000485650.1:n.-54A>T
ENST00000623115.3:c.-209A>T	ENSP00000485321.1:n.-209A>T
ENST00000623318.1:c.-54A>T	ENSP00000485423.1:n.-54A>T
ENST00000623788.1:n.545A>T
NM_000124.3:c.1546A>T	NP_000115.1:p.Arg516Trp
NM_001346440.1:c.1546A>T	NP_001333369.1:p.Arg516Trp
NM_000124.4:c.1546A>T MANE Select	NP_000115.1:p.Arg516Trp
NM_001346440.2:c.1546A>T	NP_001333369.1:p.Arg516Trp