Canonical Allele Identifier: CA376717449

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50679058A>C (hg19) ; chr10:g.49471012A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49471012A>C , CM000672.2:g.49471012A>C	GRCh38
NC_000010.10:g.50679058A>C , CM000672.1:g.50679058A>C	GRCh37
NC_000010.9:g.50349064A>C	NCBI36
NG_009442.1:g.73090T>G , LRG_465:g.73090T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.3033T>G MANE Select	ENSP00000348089.5:p.Asp1011Glu
ENST00000679552.1:n.142-123T>G
ENST00000679871.1:n.179T>G
ENST00000679974.1:n.120-123T>G
ENST00000681632.1:n.4436T>G
ENST00000681659.1:c.2874T>G	ENSP00000505631.1:p.Asp958Glu
ENST00000355832.9:c.3033T>G	ENSP00000348089.5:p.Asp1011Glu
ENST00000623073.3:c.*1329T>G	ENSP00000485650.1:n.*1329T>G
ENST00000623115.3:c.1143T>G	ENSP00000485321.1:p.Asp381Glu
ENST00000624341.3:c.865T>G
NM_000124.3:c.3033T>G	NP_000115.1:p.Asp1011Glu
XR_945953.1:n.243-553A>C
NM_001346440.1:c.3033T>G	NP_001333369.1:p.Asp1011Glu
NM_000124.4:c.3033T>G MANE Select	NP_000115.1:p.Asp1011Glu
NM_001346440.2:c.3033T>G	NP_001333369.1:p.Asp1011Glu