Canonical Allele Identifier: CA376708365

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50669486G>T (hg19) ; chr10:g.49461440G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461440G>T , CM000672.2:g.49461440G>T	GRCh38
NC_000010.10:g.50669486G>T , CM000672.1:g.50669486G>T	GRCh37
NC_000010.9:g.50339492G>T	NCBI36
NG_009442.1:g.82662C>A , LRG_465:g.82662C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3895C>A MANE Select	ENSP00000348089.5:p.Leu1299Ile
ENST00000679552.1:n.966C>A
ENST00000679871.1:n.1041C>A
ENST00000679974.1:n.944C>A
ENST00000681632.1:n.5298C>A
ENST00000681659.1:c.3736C>A	ENSP00000505631.1:p.Leu1246Ile
ENST00000355832.9:c.3895C>A	ENSP00000348089.5:p.Leu1299Ile
ENST00000465653.1:n.217C>A
ENST00000623073.3:c.*2191C>A	ENSP00000485650.1:n.*2191C>A
ENST00000623115.3:c.2005C>A	ENSP00000485321.1:p.Leu669Ile
ENST00000624341.3:c.1727C>A
NM_000124.3:c.3895C>A	NP_000115.1:p.Leu1299Ile
XR_945953.1:n.243-10125G>T
NM_001346440.1:c.3895C>A	NP_001333369.1:p.Leu1299Ile
NM_000124.4:c.3895C>A MANE Select	NP_000115.1:p.Leu1299Ile
NM_001346440.2:c.3895C>A	NP_001333369.1:p.Leu1299Ile