Canonical Allele Identifier: CA376724270

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50690801G>C (hg19) ; chr10:g.49482755G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49482755G>C , CM000672.2:g.49482755G>C	GRCh38
NC_000010.10:g.50690801G>C , CM000672.1:g.50690801G>C	GRCh37
NC_000010.9:g.50360807G>C	NCBI36
NG_009442.1:g.61347C>G , LRG_465:g.61347C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.2101C>G MANE Select	ENSP00000348089.5:p.Pro701Ala
ENST00000681632.1:n.2179C>G
ENST00000681659.1:c.1942C>G	ENSP00000505631.1:p.Pro648Ala
ENST00000355832.9:c.2101C>G	ENSP00000348089.5:p.Pro701Ala
ENST00000623073.3:c.*493C>G	ENSP00000485650.1:n.*493C>G
ENST00000623115.3:c.211C>G	ENSP00000485321.1:p.Pro71Ala
NM_000124.3:c.2101C>G	NP_000115.1:p.Pro701Ala
NM_001346440.1:c.2101C>G	NP_001333369.1:p.Pro701Ala
NM_000124.4:c.2101C>G MANE Select	NP_000115.1:p.Pro701Ala
NM_001346440.2:c.2101C>G	NP_001333369.1:p.Pro701Ala