Canonical Allele Identifier: CA3811176
Community Standard Title: NM_000287.4(PEX6):c.1941C>A (p.Cys647Ter)
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42966802G>T , CM000668.2:g.42966802G>T GRCh38
NC_000006.11:g.42934540G>T , CM000668.1:g.42934540G>T GRCh37
NC_000006.10:g.43042518G>T NCBI36
NG_008370.1:g.17442C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000287.4:c.1941C>A MANE Select NP_000278.3:p.Cys647Ter
ENST00000304611.13:c.1941C>A MANE Select ENSP00000303511.8:p.Cys647Ter
NM_000287.3:c.1941C>A NP_000278.3:p.Cys647Ter
NM_001316313.1:c.1677C>A NP_001303242.1:p.Cys559Ter
NM_001316313.2:c.1677C>A NP_001303242.1:p.Cys559Ter
NR_133009.1:n.2034C>A
NR_133009.2:n.1972C>A
ENST00000244546.4:c.1941C>A ENSP00000244546.4:p.Cys647Ter
ENST00000304611.12:c.1941C>A ENSP00000303511.8:p.Cys647Ter
XM_011514661.1:c.1857C>A XP_011512963.1:p.Cys619Ter
XM_011514661.2:c.1857C>A XP_011512963.1:p.Cys619Ter
XR_001743466.2:n.2903C>A
XR_926246.1:n.1922C>A