Canonical Allele Identifier: CA469788977

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50679049C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49471003C>T , CM000672.2:g.49471003C>T	GRCh38
NC_000010.10:g.50679049C>T , CM000672.1:g.50679049C>T	GRCh37
NC_000010.9:g.50349055C>T	NCBI36
NG_009442.1:g.73099G>A , LRG_465:g.73099G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3042G>A MANE Select	ENSP00000348089.5:p.Gln1014=
ENST00000679552.1:n.142-114G>A
ENST00000679871.1:n.188G>A
ENST00000679974.1:n.120-114G>A
ENST00000681632.1:n.4445G>A
ENST00000681659.1:c.2883G>A	ENSP00000505631.1:p.Gln961=
ENST00000355832.9:c.3042G>A	ENSP00000348089.5:p.Gln1014=
ENST00000623073.3:c.*1338G>A	ENSP00000485650.1:n.*1338G>A
ENST00000623115.3:c.1152G>A	ENSP00000485321.1:p.Gln384=
ENST00000624341.3:c.874G>A
NM_000124.3:c.3042G>A	NP_000115.1:p.Gln1014=
XR_945953.1:n.243-562C>T
NM_001346440.1:c.3042G>A	NP_001333369.1:p.Gln1014=
NM_000124.4:c.3042G>A MANE Select	NP_000115.1:p.Gln1014=
NM_001346440.2:c.3042G>A	NP_001333369.1:p.Gln1014=