Canonical Allele Identifier: CA364153613
Community Standard Title: NM_000287.4(PEX6):c.1790C>G (p.Ser597Ter)
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42967462G>C , CM000668.2:g.42967462G>C GRCh38
NC_000006.11:g.42935200G>C , CM000668.1:g.42935200G>C GRCh37
NC_000006.10:g.43043178G>C NCBI36
NG_008370.1:g.16782C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000287.4:c.1790C>G MANE Select NP_000278.3:p.Ser597Ter
ENST00000304611.13:c.1790C>G MANE Select ENSP00000303511.8:p.Ser597Ter
NM_000287.3:c.1790C>G NP_000278.3:p.Ser597Ter
NM_001316313.1:c.1526C>G NP_001303242.1:p.Ser509Ter
NM_001316313.2:c.1526C>G NP_001303242.1:p.Ser509Ter
NR_133009.1:n.1883C>G
NR_133009.2:n.1821C>G
ENST00000244546.4:c.1790C>G ENSP00000244546.4:p.Ser597Ter
ENST00000304611.12:c.1790C>G ENSP00000303511.8:p.Ser597Ter
XM_011514661.1:c.1706C>G XP_011512963.1:p.Ser569Ter
XM_011514661.2:c.1706C>G XP_011512963.1:p.Ser569Ter
XR_001743466.2:n.2752C>G
XR_926246.1:n.1771C>G