Canonical Allele Identifier: CA376755054
Gene: ERCC6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49524676T>C , CM000672.2:g.49524676T>C GRCh38
NC_000010.10:g.50732722T>C , CM000672.1:g.50732722T>C GRCh37
NC_000010.9:g.50402728T>C NCBI36
NG_009442.1:g.19426A>G , LRG_465:g.19426A>G
NG_033155.1:g.4606A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355832.10:c.754A>G MANE Select ENSP00000348089.5:p.Ile252Val
ENST00000447839.7:c.754A>G MANE Plus Clinical ENSP00000387966.2:p.Ile252Val
ENST00000679596.1:c.*383A>G ENSP00000504862.1:n.*383A>G
ENST00000679811.1:n.837A>G
ENST00000680107.1:c.652+3741A>G ENSP00000505909.1:n.652+3741A>G
ENST00000680233.1:n.847A>G
ENST00000681632.1:n.832A>G
ENST00000681659.1:c.754A>G ENSP00000505631.1:p.Ile252Val
ENST00000355832.9:c.754A>G ENSP00000348089.5:p.Ile252Val
ENST00000447839.6:c.754A>G ENSP00000387966.2:p.Ile252Val
ENST00000515869.1:c.754A>G ENSP00000423550.1:p.Ile252Val
NM_000124.3:c.754A>G NP_000115.1:p.Ile252Val
NM_001277058.1:c.754A>G NP_001263987.1:p.Ile252Val
NM_001277059.1:c.754A>G NP_001263988.1:p.Ile252Val
NM_001346440.1:c.754A>G NP_001333369.1:p.Ile252Val
NM_000124.4:c.754A>G MANE Select NP_000115.1:p.Ile252Val
NM_001277058.2:c.754A>G MANE Plus Clinical NP_001263987.1:p.Ile252Val
NM_001277059.2:c.754A>G NP_001263988.1:p.Ile252Val
NM_001346440.2:c.754A>G NP_001333369.1:p.Ile252Val