Canonical Allele Identifier: CA376713301

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50678385C>G (hg19) ; chr10:g.49470339C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470339C>G , CM000672.2:g.49470339C>G	GRCh38
NC_000010.10:g.50678385C>G , CM000672.1:g.50678385C>G	GRCh37
NC_000010.9:g.50348391C>G	NCBI36
NG_009442.1:g.73763G>C , LRG_465:g.73763G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3621G>C MANE Select	ENSP00000348089.5:p.Lys1207Asn
ENST00000679552.1:n.692G>C
ENST00000679871.1:n.767G>C
ENST00000679974.1:n.670G>C
ENST00000681632.1:n.5024G>C
ENST00000681659.1:c.3462G>C	ENSP00000505631.1:p.Lys1154Asn
ENST00000355832.9:c.3621G>C	ENSP00000348089.5:p.Lys1207Asn
ENST00000623073.3:c.*1917G>C	ENSP00000485650.1:n.*1917G>C
ENST00000623115.3:c.1731G>C	ENSP00000485321.1:p.Lys577Asn
ENST00000624341.3:c.1453G>C
NM_000124.3:c.3621G>C	NP_000115.1:p.Lys1207Asn
XR_945953.1:n.243-1226C>G
NM_001346440.1:c.3621G>C	NP_001333369.1:p.Lys1207Asn
NM_000124.4:c.3621G>C MANE Select	NP_000115.1:p.Lys1207Asn
NM_001346440.2:c.3621G>C	NP_001333369.1:p.Lys1207Asn