Canonical Allele Identifier: CA138221658
Community Standard Title: NM_000287.4(PEX6):c.2663G>C (p.Arg888Pro)
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42965078C>G , CM000668.2:g.42965078C>G GRCh38
NC_000006.11:g.42932816C>G , CM000668.1:g.42932816C>G GRCh37
NC_000006.10:g.43040794C>G NCBI36
NG_008370.1:g.19166G>C
NG_008396.1:g.9317C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000287.4:c.2663G>C MANE Select NP_000278.3:p.Arg888Pro
ENST00000304611.13:c.2663G>C MANE Select ENSP00000303511.8:p.Arg888Pro
NM_000287.3:c.2663G>C NP_000278.3:p.Arg888Pro
NM_001316313.1:c.2399G>C NP_001303242.1:p.Arg800Pro
NM_001316313.2:c.2399G>C NP_001303242.1:p.Arg800Pro
NR_133009.1:n.2509G>C
NR_133009.2:n.2447G>C
ENST00000244546.4:c.2416G>C ENSP00000244546.4:n.2416G>C
ENST00000304611.12:c.2663G>C ENSP00000303511.8:p.Arg888Pro
XM_011514661.1:c.2579G>C XP_011512963.1:p.Arg860Pro
XM_011514661.2:c.2579G>C XP_011512963.1:p.Arg860Pro
XR_001743466.2:n.3625G>C