Canonical Allele Identifier: CA2678796845
Gene: PEX6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42969878del , CM000668.2:g.42969878del GRCh38
NC_000006.11:g.42937616del , CM000668.1:g.42937616del GRCh37
NC_000006.10:g.43045594del NCBI36
NG_008370.1:g.14369del

Transcript Alleles

HGVS Amino-acid Change
ENST00000304611.13:c.1233+10del MANE Select ENSP00000303511.8:n.1233+10del
ENST00000244546.4:c.1233+10del ENSP00000244546.4:n.1233+10del
ENST00000304611.12:c.1233+10del ENSP00000303511.8:n.1233+10del
NM_000287.3:c.1233+10del NP_000278.3:n.1233+10del
NM_001316313.1:c.969+10del NP_001303242.1:n.969+10del
NR_133009.1:n.1326+10del
XM_011514661.1:c.1149+10del XP_011512963.1:n.1149+10del
XR_926246.1:n.1326+10del
XM_011514661.2:c.1149+10del XP_011512963.1:n.1149+10del
XR_001743466.2:n.2307+10del
NM_000287.4:c.1233+10del MANE Select NP_000278.3:n.1233+10del
NM_001316313.2:c.969+10del NP_001303242.1:n.969+10del
NR_133009.2:n.1264+10del