Canonical Allele Identifier: CA380223393

Gene: PEX16

Linked Data

• MyVariant Identifiers: chr11:g.45931839G>T (hg19) ; chr11:g.45910288G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910288G>T , CM000673.2:g.45910288G>T	GRCh38
NC_000011.9:g.45931839G>T , CM000673.1:g.45931839G>T	GRCh37
NC_000011.8:g.45888415G>T	NCBI36
NG_008460.1:g.12836C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.977C>A MANE Select	ENSP00000368024.5:p.Thr326Asn
ENST00000241041.7:c.953-111C>A	ENSP00000241041.3:n.953-111C>A
ENST00000378750.9:c.977C>A	ENSP00000368024.5:p.Thr326Asn
ENST00000523721.2:n.207C>A
ENST00000532681.5:c.692C>A	ENSP00000434654.1:p.Thr231Asn
NM_004813.2:c.977C>A	NP_004804.1:p.Thr326Asn
NM_057174.2:c.953-111C>A	NP_476515.1:n.953-111C>A
XM_011520474.1:c.854C>A	XP_011518776.1:p.Thr285Asn
NM_004813.3:c.977C>A	NP_004804.1:p.Thr326Asn
NM_004813.4:c.977C>A MANE Select	NP_004804.2:p.Thr326Asn
NM_057174.3:c.953-111C>A	NP_476515.2:n.953-111C>A