Canonical Allele Identifier: CA364151080
Community Standard Title: NM_000287.4(PEX6):c.2518C>T (p.Gln840Ter)
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42965322G>A , CM000668.2:g.42965322G>A GRCh38
NC_000006.11:g.42933060G>A , CM000668.1:g.42933060G>A GRCh37
NC_000006.10:g.43041038G>A NCBI36
NG_008370.1:g.18922C>T
NG_008396.1:g.9561G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000287.4:c.2518C>T MANE Select NP_000278.3:p.Gln840Ter
ENST00000304611.13:c.2518C>T MANE Select ENSP00000303511.8:p.Gln840Ter
NM_000287.3:c.2518C>T NP_000278.3:p.Gln840Ter
NM_001316313.1:c.2254C>T NP_001303242.1:p.Gln752Ter
NM_001316313.2:c.2254C>T NP_001303242.1:p.Gln752Ter
NR_133009.1:n.2364C>T
NR_133009.2:n.2302C>T
ENST00000244546.4:c.2271C>T ENSP00000244546.4:n.2271C>T
ENST00000304611.12:c.2518C>T ENSP00000303511.8:p.Gln840Ter
XM_011514661.1:c.2434C>T XP_011512963.1:p.Gln812Ter
XM_011514661.2:c.2434C>T XP_011512963.1:p.Gln812Ter
XR_001743466.2:n.3480C>T