Canonical Allele Identifier: CA376708152

Gene: ERCC6

Linked Data

• gnomAD v4: 10-49460438-T-C
• MyVariant Identifiers: chr10:g.50668484T>C (hg19) ; chr10:g.49460438T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49460438T>C , CM000672.2:g.49460438T>C	GRCh38
NC_000010.10:g.50668484T>C , CM000672.1:g.50668484T>C	GRCh37
NC_000010.9:g.50338490T>C	NCBI36
NG_009442.1:g.83664A>G , LRG_465:g.83664A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.3997A>G MANE Select	ENSP00000348089.5:p.Lys1333Glu
ENST00000679552.1:n.1068A>G
ENST00000679871.1:n.1143A>G
ENST00000679974.1:n.1046A>G
ENST00000681632.1:n.5400A>G
ENST00000681659.1:c.3838A>G	ENSP00000505631.1:p.Lys1280Glu
ENST00000355832.9:c.3997A>G	ENSP00000348089.5:p.Lys1333Glu
ENST00000465653.1:n.319A>G
ENST00000623073.3:c.*2293A>G	ENSP00000485650.1:n.*2293A>G
ENST00000623115.3:c.2107A>G	ENSP00000485321.1:p.Lys703Glu
ENST00000624341.3:c.1829A>G
NM_000124.3:c.3997A>G	NP_000115.1:p.Lys1333Glu
XR_945953.1:n.243-11127T>C
NM_001346440.1:c.3997A>G	NP_001333369.1:p.Lys1333Glu
NM_000124.4:c.3997A>G MANE Select	NP_000115.1:p.Lys1333Glu
NM_001346440.2:c.3997A>G	NP_001333369.1:p.Lys1333Glu