Canonical Allele Identifier: CA1968698313
Gene: PEX16 HGNC NCBI

Linked Data

dbSNP Id: rs2086764317

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45910397C>T , CM000673.2:g.45910397C>T GRCh38
NC_000011.9:g.45931948C>T , CM000673.1:g.45931948C>T GRCh37
NC_000011.8:g.45888524C>T NCBI36
NG_008460.1:g.12727G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378750.10:c.953-85G>A MANE Select ENSP00000368024.5:n.953-85G>A
ENST00000241041.7:c.953-220G>A ENSP00000241041.3:n.953-220G>A
ENST00000378750.9:c.953-85G>A ENSP00000368024.5:n.953-85G>A
ENST00000523721.2:n.183-85G>A
ENST00000532681.5:c.668-85G>A ENSP00000434654.1:n.668-85G>A
NM_004813.2:c.953-85G>A NP_004804.1:n.953-85G>A
NM_057174.2:c.953-220G>A NP_476515.1:n.953-220G>A
XM_011520474.1:c.830-85G>A XP_011518776.1:n.830-85G>A
NM_004813.3:c.953-85G>A NP_004804.1:n.953-85G>A
NM_004813.4:c.953-85G>A MANE Select NP_004804.2:n.953-85G>A
NM_057174.3:c.953-220G>A NP_476515.2:n.953-220G>A