Canonical Allele Identifier: CA2574806427
Gene: PEX16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45910364T>C , CM000673.2:g.45910364T>C GRCh38
NC_000011.9:g.45931915T>C , CM000673.1:g.45931915T>C GRCh37
NC_000011.8:g.45888491T>C NCBI36
NG_008460.1:g.12760A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378750.10:c.953-52A>G MANE Select ENSP00000368024.5:n.953-52A>G
ENST00000241041.7:c.953-187A>G ENSP00000241041.3:n.953-187A>G
ENST00000378750.9:c.953-52A>G ENSP00000368024.5:n.953-52A>G
ENST00000523721.2:n.183-52A>G
ENST00000532681.5:c.668-52A>G ENSP00000434654.1:n.668-52A>G
NM_004813.2:c.953-52A>G NP_004804.1:n.953-52A>G
NM_057174.2:c.953-187A>G NP_476515.1:n.953-187A>G
XM_011520474.1:c.830-52A>G XP_011518776.1:n.830-52A>G
NM_004813.3:c.953-52A>G NP_004804.1:n.953-52A>G
NM_004813.4:c.953-52A>G MANE Select NP_004804.2:n.953-52A>G
NM_057174.3:c.953-187A>G NP_476515.2:n.953-187A>G