Canonical Allele Identifier: CA469604516

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50701223C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49493177C>G , CM000672.2:g.49493177C>G	GRCh38
NC_000010.10:g.50701223C>G , CM000672.1:g.50701223C>G	GRCh37
NC_000010.9:g.50371229C>G	NCBI36
NG_009442.1:g.50925G>C , LRG_465:g.50925G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.1761G>C MANE Select	ENSP00000348089.5:p.Thr587=
ENST00000681632.1:n.1839G>C
ENST00000681659.1:c.1602G>C	ENSP00000505631.1:p.Thr534=
ENST00000355832.9:c.1761G>C	ENSP00000348089.5:p.Thr587=
ENST00000475116.1:n.275+7361G>C
ENST00000623073.3:c.162G>C	ENSP00000485650.1:p.Thr54=
ENST00000623115.3:c.-70+7361G>C	ENSP00000485321.1:n.-70+7361G>C
ENST00000623318.1:c.162G>C	ENSP00000485423.1:p.Thr54=
NM_000124.3:c.1761G>C	NP_000115.1:p.Thr587=
NM_001346440.1:c.1761G>C	NP_001333369.1:p.Thr587=
NM_000124.4:c.1761G>C MANE Select	NP_000115.1:p.Thr587=
NM_001346440.2:c.1761G>C	NP_001333369.1:p.Thr587=