Canonical Allele Identifier: CA364169296
Community Standard Title: NM_000287.4(PEX6):c.87G>A (p.Trp29Ter)
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42979064C>T , CM000668.2:g.42979064C>T GRCh38
NC_000006.11:g.42946802C>T , CM000668.1:g.42946802C>T GRCh37
NC_000006.10:g.43054780C>T NCBI36
NG_008370.1:g.5180G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000287.4:c.87G>A MANE Select NP_000278.3:p.Trp29Ter
ENST00000304611.13:c.87G>A MANE Select ENSP00000303511.8:p.Trp29Ter
NM_000287.3:c.87G>A NP_000278.3:p.Trp29Ter
NM_001316313.1:c.87G>A NP_001303242.1:p.Trp29Ter
NM_001316313.2:c.87G>A NP_001303242.1:p.Trp29Ter
NR_133009.1:n.180G>A
NR_133009.2:n.118G>A
ENST00000244546.4:c.87G>A ENSP00000244546.4:p.Trp29Ter
ENST00000304611.12:c.87G>A ENSP00000303511.8:p.Trp29Ter
XM_011514661.1:c.87G>A XP_011512963.1:p.Trp29Ter
XM_011514661.2:c.87G>A XP_011512963.1:p.Trp29Ter
XR_001743466.2:n.1161G>A
XR_926246.1:n.180G>A