Canonical Allele Identifier: CA2791291475
Gene: PEX16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45910392_45910397del , CM000673.2:g.45910392_45910397del GRCh38
NC_000011.9:g.45931943_45931948del , CM000673.1:g.45931943_45931948del GRCh37
NC_000011.8:g.45888519_45888524del NCBI36
NG_008460.1:g.12727_12732del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378750.10:c.953-85_953-80del MANE Select ENSP00000368024.5:n.953-85_953-80del
ENST00000241041.7:c.953-220_953-215del ENSP00000241041.3:n.953-220_953-215del
ENST00000378750.9:c.953-85_953-80del ENSP00000368024.5:n.953-85_953-80del
ENST00000523721.2:n.183-85_183-80del
ENST00000532681.5:c.668-85_668-80del ENSP00000434654.1:n.668-85_668-80del
NM_004813.2:c.953-85_953-80del NP_004804.1:n.953-85_953-80del
NM_057174.2:c.953-220_953-215del NP_476515.1:n.953-220_953-215del
XM_011520474.1:c.830-85_830-80del XP_011518776.1:n.830-85_830-80del
NM_004813.3:c.953-85_953-80del NP_004804.1:n.953-85_953-80del
NM_004813.4:c.953-85_953-80del MANE Select NP_004804.2:n.953-85_953-80del
NM_057174.3:c.953-220_953-215del NP_476515.2:n.953-220_953-215del