Canonical Allele Identifier: CA469604019

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50690805C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49482759C>A , CM000672.2:g.49482759C>A	GRCh38
NC_000010.10:g.50690805C>A , CM000672.1:g.50690805C>A	GRCh37
NC_000010.9:g.50360811C>A	NCBI36
NG_009442.1:g.61343G>T , LRG_465:g.61343G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.2097G>T MANE Select	ENSP00000348089.5:p.Thr699=
ENST00000681632.1:n.2175G>T
ENST00000681659.1:c.1938G>T	ENSP00000505631.1:p.Thr646=
ENST00000355832.9:c.2097G>T	ENSP00000348089.5:p.Thr699=
ENST00000623073.3:c.*489G>T	ENSP00000485650.1:n.*489G>T
ENST00000623115.3:c.207G>T	ENSP00000485321.1:p.Thr69=
NM_000124.3:c.2097G>T	NP_000115.1:p.Thr699=
NM_001346440.1:c.2097G>T	NP_001333369.1:p.Thr699=
NM_000124.4:c.2097G>T MANE Select	NP_000115.1:p.Thr699=
NM_001346440.2:c.2097G>T	NP_001333369.1:p.Thr699=