Canonical Allele Identifier: CA380223466

Gene: PEX16

Linked Data

• MyVariant Identifiers: chr11:g.45931849A>T (hg19) ; chr11:g.45910298A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910298A>T , CM000673.2:g.45910298A>T	GRCh38
NC_000011.9:g.45931849A>T , CM000673.1:g.45931849A>T	GRCh37
NC_000011.8:g.45888425A>T	NCBI36
NG_008460.1:g.12826T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.967T>A MANE Select	ENSP00000368024.5:p.Tyr323Asn
ENST00000241041.7:c.953-121T>A	ENSP00000241041.3:n.953-121T>A
ENST00000378750.9:c.967T>A	ENSP00000368024.5:p.Tyr323Asn
ENST00000523721.2:n.197T>A
ENST00000532681.5:c.682T>A	ENSP00000434654.1:p.Tyr228Asn
NM_004813.2:c.967T>A	NP_004804.1:p.Tyr323Asn
NM_057174.2:c.953-121T>A	NP_476515.1:n.953-121T>A
XM_011520474.1:c.844T>A	XP_011518776.1:p.Tyr282Asn
NM_004813.3:c.967T>A	NP_004804.1:p.Tyr323Asn
NM_004813.4:c.967T>A MANE Select	NP_004804.2:p.Tyr323Asn
NM_057174.3:c.953-121T>A	NP_476515.2:n.953-121T>A