Canonical Allele Identifier: CA469600300

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50669448A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461402A>C , CM000672.2:g.49461402A>C	GRCh38
NC_000010.10:g.50669448A>C , CM000672.1:g.50669448A>C	GRCh37
NC_000010.9:g.50339454A>C	NCBI36
NG_009442.1:g.82700T>G , LRG_465:g.82700T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3933T>G MANE Select	ENSP00000348089.5:p.Val1311=
ENST00000679552.1:n.1004T>G
ENST00000679871.1:n.1079T>G
ENST00000679974.1:n.982T>G
ENST00000681632.1:n.5336T>G
ENST00000681659.1:c.3774T>G	ENSP00000505631.1:p.Val1258=
ENST00000355832.9:c.3933T>G	ENSP00000348089.5:p.Val1311=
ENST00000465653.1:n.255T>G
ENST00000623073.3:c.*2229T>G	ENSP00000485650.1:n.*2229T>G
ENST00000623115.3:c.2043T>G	ENSP00000485321.1:p.Val681=
ENST00000624341.3:c.1765T>G
NM_000124.3:c.3933T>G	NP_000115.1:p.Val1311=
XR_945953.1:n.243-10163A>C
NM_001346440.1:c.3933T>G	NP_001333369.1:p.Val1311=
NM_000124.4:c.3933T>G MANE Select	NP_000115.1:p.Val1311=
NM_001346440.2:c.3933T>G	NP_001333369.1:p.Val1311=