Canonical Allele Identifier: CA469600358

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50669523G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461477G>T , CM000672.2:g.49461477G>T	GRCh38
NC_000010.10:g.50669523G>T , CM000672.1:g.50669523G>T	GRCh37
NC_000010.9:g.50339529G>T	NCBI36
NG_009442.1:g.82625C>A , LRG_465:g.82625C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.3858C>A MANE Select	ENSP00000348089.5:p.Ala1286=
ENST00000679552.1:n.929C>A
ENST00000679871.1:n.1004C>A
ENST00000679974.1:n.907C>A
ENST00000681632.1:n.5261C>A
ENST00000681659.1:c.3699C>A	ENSP00000505631.1:p.Ala1233=
ENST00000355832.9:c.3858C>A	ENSP00000348089.5:p.Ala1286=
ENST00000465653.1:n.180C>A
ENST00000623073.3:c.*2154C>A	ENSP00000485650.1:n.*2154C>A
ENST00000623115.3:c.1968C>A	ENSP00000485321.1:p.Ala656=
ENST00000624341.3:c.1690C>A
NM_000124.3:c.3858C>A	NP_000115.1:p.Ala1286=
XR_945953.1:n.243-10088G>T
NM_001346440.1:c.3858C>A	NP_001333369.1:p.Ala1286=
NM_000124.4:c.3858C>A MANE Select	NP_000115.1:p.Ala1286=
NM_001346440.2:c.3858C>A	NP_001333369.1:p.Ala1286=