Canonical Allele Identifier: CA3811146
Community Standard Title: NM_000287.4(PEX6):c.1992G>C (p.Glu664Asp)
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42966627C>G , CM000668.2:g.42966627C>G GRCh38
NC_000006.11:g.42934365C>G , CM000668.1:g.42934365C>G GRCh37
NC_000006.10:g.43042343C>G NCBI36
NG_008370.1:g.17617G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000287.4:c.1992G>C MANE Select NP_000278.3:p.Glu664Asp
ENST00000304611.13:c.1992G>C MANE Select ENSP00000303511.8:p.Glu664Asp
NM_000287.3:c.1992G>C NP_000278.3:p.Glu664Asp
NM_001316313.1:c.1728G>C NP_001303242.1:p.Glu576Asp
NM_001316313.2:c.1728G>C NP_001303242.1:p.Glu576Asp
NR_133009.1:n.2085G>C
NR_133009.2:n.2023G>C
ENST00000244546.4:c.1992G>C ENSP00000244546.4:p.Glu664Asp
ENST00000304611.12:c.1992G>C ENSP00000303511.8:p.Glu664Asp
XM_011514661.1:c.1908G>C XP_011512963.1:p.Glu636Asp
XM_011514661.2:c.1908G>C XP_011512963.1:p.Glu636Asp
XR_001743466.2:n.2954G>C
XR_926246.1:n.1973G>C