Canonical Allele Identifier: CA937547705
Gene: PEX16 HGNC NCBI

Linked Data

dbSNP Id: rs2086764075

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45910389del , CM000673.2:g.45910389del GRCh38
NC_000011.9:g.45931940del , CM000673.1:g.45931940del GRCh37
NC_000011.8:g.45888516del NCBI36
NG_008460.1:g.12738del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378750.10:c.953-74del MANE Select ENSP00000368024.5:n.953-74del
ENST00000241041.7:c.953-209del ENSP00000241041.3:n.953-209del
ENST00000378750.9:c.953-74del ENSP00000368024.5:n.953-74del
ENST00000523721.2:n.183-74del
ENST00000532681.5:c.668-74del ENSP00000434654.1:n.668-74del
NM_004813.2:c.953-74del NP_004804.1:n.953-74del
NM_057174.2:c.953-209del NP_476515.1:n.953-209del
XM_011520474.1:c.830-74del XP_011518776.1:n.830-74del
NM_004813.3:c.953-74del NP_004804.1:n.953-74del
NM_004813.4:c.953-74del MANE Select NP_004804.2:n.953-74del
NM_057174.3:c.953-209del NP_476515.2:n.953-209del