Canonical Allele Identifier: CA469790825

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50732759G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49524713G>C , CM000672.2:g.49524713G>C	GRCh38
NC_000010.10:g.50732759G>C , CM000672.1:g.50732759G>C	GRCh37
NC_000010.9:g.50402765G>C	NCBI36
NG_009442.1:g.19389C>G , LRG_465:g.19389C>G
NG_033155.1:g.4569C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.717C>G MANE Select	ENSP00000348089.5:p.Leu239=
ENST00000447839.7:c.717C>G MANE Plus Clinical	ENSP00000387966.2:p.Leu239=
ENST00000679596.1:c.*346C>G	ENSP00000504862.1:n.*346C>G
ENST00000679811.1:n.800C>G
ENST00000680107.1:c.652+3704C>G	ENSP00000505909.1:n.652+3704C>G
ENST00000680233.1:n.810C>G
ENST00000681632.1:n.795C>G
ENST00000681659.1:c.717C>G	ENSP00000505631.1:p.Leu239=
ENST00000355832.9:c.717C>G	ENSP00000348089.5:p.Leu239=
ENST00000447839.6:c.717C>G	ENSP00000387966.2:p.Leu239=
ENST00000515869.1:c.717C>G	ENSP00000423550.1:p.Leu239=
NM_000124.3:c.717C>G	NP_000115.1:p.Leu239=
NM_001277058.1:c.717C>G	NP_001263987.1:p.Leu239=
NM_001277059.1:c.717C>G	NP_001263988.1:p.Leu239=
NM_001346440.1:c.717C>G	NP_001333369.1:p.Leu239=
NM_000124.4:c.717C>G MANE Select	NP_000115.1:p.Leu239=
NM_001277058.2:c.717C>G MANE Plus Clinical	NP_001263987.1:p.Leu239=
NM_001277059.2:c.717C>G	NP_001263988.1:p.Leu239=
NM_001346440.2:c.717C>G	NP_001333369.1:p.Leu239=