Canonical Allele Identifier: CA376754104

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50732580G>C (hg19) ; chr10:g.49524534G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49524534G>C , CM000672.2:g.49524534G>C	GRCh38
NC_000010.10:g.50732580G>C , CM000672.1:g.50732580G>C	GRCh37
NC_000010.9:g.50402586G>C	NCBI36
NG_009442.1:g.19568C>G , LRG_465:g.19568C>G
NG_033155.1:g.4748C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.896C>G MANE Select	ENSP00000348089.5:p.Pro299Arg
ENST00000447839.7:c.896C>G MANE Plus Clinical	ENSP00000387966.2:p.Pro299Arg
ENST00000679596.1:c.*525C>G	ENSP00000504862.1:n.*525C>G
ENST00000679811.1:n.979C>G
ENST00000680107.1:c.652+3883C>G	ENSP00000505909.1:n.652+3883C>G
ENST00000680233.1:n.989C>G
ENST00000681632.1:n.974C>G
ENST00000681659.1:c.896C>G	ENSP00000505631.1:p.Pro299Arg
ENST00000355832.9:c.896C>G	ENSP00000348089.5:p.Pro299Arg
ENST00000447839.6:c.896C>G	ENSP00000387966.2:p.Pro299Arg
ENST00000515869.1:c.896C>G	ENSP00000423550.1:p.Pro299Arg
NM_000124.3:c.896C>G	NP_000115.1:p.Pro299Arg
NM_001277058.1:c.896C>G	NP_001263987.1:p.Pro299Arg
NM_001277059.1:c.896C>G	NP_001263988.1:p.Pro299Arg
NM_001346440.1:c.896C>G	NP_001333369.1:p.Pro299Arg
NM_000124.4:c.896C>G MANE Select	NP_000115.1:p.Pro299Arg
NM_001277058.2:c.896C>G MANE Plus Clinical	NP_001263987.1:p.Pro299Arg
NM_001277059.2:c.896C>G	NP_001263988.1:p.Pro299Arg
NM_001346440.2:c.896C>G	NP_001333369.1:p.Pro299Arg