Canonical Allele Identifier: CA364156011
Gene: PEX6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42969888G>T , CM000668.2:g.42969888G>T GRCh38
NC_000006.11:g.42937626G>T , CM000668.1:g.42937626G>T GRCh37
NC_000006.10:g.43045604G>T NCBI36
NG_008370.1:g.14356C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000304611.13:c.1230C>A MANE Select ENSP00000303511.8:p.Tyr410Ter
ENST00000244546.4:c.1230C>A ENSP00000244546.4:p.Tyr410Ter
ENST00000304611.12:c.1230C>A ENSP00000303511.8:p.Tyr410Ter
NM_000287.3:c.1230C>A NP_000278.3:p.Tyr410Ter
NM_001316313.1:c.966C>A NP_001303242.1:p.Tyr322Ter
NR_133009.1:n.1323C>A
XM_011514661.1:c.1146C>A XP_011512963.1:p.Tyr382Ter
XR_926246.1:n.1323C>A
XM_011514661.2:c.1146C>A XP_011512963.1:p.Tyr382Ter
XR_001743466.2:n.2304C>A
NM_000287.4:c.1230C>A MANE Select NP_000278.3:p.Tyr410Ter
NM_001316313.2:c.966C>A NP_001303242.1:p.Tyr322Ter
NR_133009.2:n.1261C>A