Canonical Allele Identifier: CA469604027

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50690817T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49482771T>G , CM000672.2:g.49482771T>G	GRCh38
NC_000010.10:g.50690817T>G , CM000672.1:g.50690817T>G	GRCh37
NC_000010.9:g.50360823T>G	NCBI36
NG_009442.1:g.61331A>C , LRG_465:g.61331A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.2085A>C MANE Select	ENSP00000348089.5:p.Gly695=
ENST00000681632.1:n.2163A>C
ENST00000681659.1:c.1926A>C	ENSP00000505631.1:p.Gly642=
ENST00000355832.9:c.2085A>C	ENSP00000348089.5:p.Gly695=
ENST00000623073.3:c.*477A>C	ENSP00000485650.1:n.*477A>C
ENST00000623115.3:c.195A>C	ENSP00000485321.1:p.Gly65=
NM_000124.3:c.2085A>C	NP_000115.1:p.Gly695=
NM_001346440.1:c.2085A>C	NP_001333369.1:p.Gly695=
NM_000124.4:c.2085A>C MANE Select	NP_000115.1:p.Gly695=
NM_001346440.2:c.2085A>C	NP_001333369.1:p.Gly695=