Canonical Allele Identifier: CA376708553

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50669547A>T (hg19) ; chr10:g.49461501A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461501A>T , CM000672.2:g.49461501A>T	GRCh38
NC_000010.10:g.50669547A>T , CM000672.1:g.50669547A>T	GRCh37
NC_000010.9:g.50339553A>T	NCBI36
NG_009442.1:g.82601T>A , LRG_465:g.82601T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3834T>A MANE Select	ENSP00000348089.5:p.Asp1278Glu
ENST00000679552.1:n.905T>A
ENST00000679871.1:n.980T>A
ENST00000679974.1:n.883T>A
ENST00000681632.1:n.5237T>A
ENST00000681659.1:c.3675T>A	ENSP00000505631.1:p.Asp1225Glu
ENST00000355832.9:c.3834T>A	ENSP00000348089.5:p.Asp1278Glu
ENST00000465653.1:n.156T>A
ENST00000623073.3:c.*2130T>A	ENSP00000485650.1:n.*2130T>A
ENST00000623115.3:c.1944T>A	ENSP00000485321.1:p.Asp648Glu
ENST00000624341.3:c.1666T>A
NM_000124.3:c.3834T>A	NP_000115.1:p.Asp1278Glu
XR_945953.1:n.243-10064A>T
NM_001346440.1:c.3834T>A	NP_001333369.1:p.Asp1278Glu
NM_000124.4:c.3834T>A MANE Select	NP_000115.1:p.Asp1278Glu
NM_001346440.2:c.3834T>A	NP_001333369.1:p.Asp1278Glu