Canonical Allele Identifier: CA376708443

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50669524G>A (hg19) ; chr10:g.49461478G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461478G>A , CM000672.2:g.49461478G>A	GRCh38
NC_000010.10:g.50669524G>A , CM000672.1:g.50669524G>A	GRCh37
NC_000010.9:g.50339530G>A	NCBI36
NG_009442.1:g.82624C>T , LRG_465:g.82624C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.3857C>T MANE Select	ENSP00000348089.5:p.Ala1286Val
ENST00000679552.1:n.928C>T
ENST00000679871.1:n.1003C>T
ENST00000679974.1:n.906C>T
ENST00000681632.1:n.5260C>T
ENST00000681659.1:c.3698C>T	ENSP00000505631.1:p.Ala1233Val
ENST00000355832.9:c.3857C>T	ENSP00000348089.5:p.Ala1286Val
ENST00000465653.1:n.179C>T
ENST00000623073.3:c.*2153C>T	ENSP00000485650.1:n.*2153C>T
ENST00000623115.3:c.1967C>T	ENSP00000485321.1:p.Ala656Val
ENST00000624341.3:c.1689C>T
NM_000124.3:c.3857C>T	NP_000115.1:p.Ala1286Val
XR_945953.1:n.243-10087G>A
NM_001346440.1:c.3857C>T	NP_001333369.1:p.Ala1286Val
NM_000124.4:c.3857C>T MANE Select	NP_000115.1:p.Ala1286Val
NM_001346440.2:c.3857C>T	NP_001333369.1:p.Ala1286Val