Canonical Allele Identifier: CA469788996

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50679058A>G (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.3033T>C MANE Select	ENSP00000348089.5:p.Asp1011=
ENST00000679552.1:n.142-123T>C
ENST00000679871.1:n.179T>C
ENST00000679974.1:n.120-123T>C
ENST00000681632.1:n.4436T>C
ENST00000681659.1:c.2874T>C	ENSP00000505631.1:p.Asp958=
ENST00000355832.9:c.3033T>C	ENSP00000348089.5:p.Asp1011=
ENST00000623073.3:c.*1329T>C	ENSP00000485650.1:n.*1329T>C
ENST00000623115.3:c.1143T>C	ENSP00000485321.1:p.Asp381=
ENST00000624341.3:c.865T>C
NM_000124.3:c.3033T>C	NP_000115.1:p.Asp1011=
XR_945953.1:n.243-553A>G
NM_001346440.1:c.3033T>C	NP_001333369.1:p.Asp1011=
NM_000124.4:c.3033T>C MANE Select	NP_000115.1:p.Asp1011=
NM_001346440.2:c.3033T>C	NP_001333369.1:p.Asp1011=