Canonical Allele Identifier: CA380223402

Gene: PEX16

Linked Data

• MyVariant Identifiers: chr11:g.45931840T>C (hg19) ; chr11:g.45910289T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910289T>C , CM000673.2:g.45910289T>C	GRCh38
NC_000011.9:g.45931840T>C , CM000673.1:g.45931840T>C	GRCh37
NC_000011.8:g.45888416T>C	NCBI36
NG_008460.1:g.12835A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.976A>G MANE Select	ENSP00000368024.5:p.Thr326Ala
ENST00000241041.7:c.953-112A>G	ENSP00000241041.3:n.953-112A>G
ENST00000378750.9:c.976A>G	ENSP00000368024.5:p.Thr326Ala
ENST00000523721.2:n.206A>G
ENST00000532681.5:c.691A>G	ENSP00000434654.1:p.Thr231Ala
NM_004813.2:c.976A>G	NP_004804.1:p.Thr326Ala
NM_057174.2:c.953-112A>G	NP_476515.1:n.953-112A>G
XM_011520474.1:c.853A>G	XP_011518776.1:p.Thr285Ala
NM_004813.3:c.976A>G	NP_004804.1:p.Thr326Ala
NM_004813.4:c.976A>G MANE Select	NP_004804.2:p.Thr326Ala
NM_057174.3:c.953-112A>G	NP_476515.2:n.953-112A>G