Canonical Allele Identifier: CA364151527
Community Standard Title: NM_000287.4(PEX6):c.2410G>C (p.Glu804Gln)
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42965742C>G , CM000668.2:g.42965742C>G GRCh38
NC_000006.11:g.42933480C>G , CM000668.1:g.42933480C>G GRCh37
NC_000006.10:g.43041458C>G NCBI36
NG_008370.1:g.18502G>C
NG_008396.1:g.9981C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000287.4:c.2410G>C MANE Select NP_000278.3:p.Glu804Gln
ENST00000304611.13:c.2410G>C MANE Select ENSP00000303511.8:p.Glu804Gln
NM_000287.3:c.2410G>C NP_000278.3:p.Glu804Gln
NM_001316313.1:c.2146G>C NP_001303242.1:p.Glu716Gln
NM_001316313.2:c.2146G>C NP_001303242.1:p.Glu716Gln
NR_133009.1:n.2256G>C
NR_133009.2:n.2194G>C
ENST00000244546.4:c.2163G>C ENSP00000244546.4:p.Met721Ile
ENST00000304611.12:c.2410G>C ENSP00000303511.8:p.Glu804Gln
XM_011514661.1:c.2326G>C XP_011512963.1:p.Glu776Gln
XM_011514661.2:c.2326G>C XP_011512963.1:p.Glu776Gln
XR_001743466.2:n.3372G>C