Canonical Allele Identifier: CA1968698300

Gene: PEX16

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910385_45910386delinsAC , CM000673.2:g.45910385_45910386delinsAC	GRCh38
NC_000011.9:g.45931936_45931937delinsAC , CM000673.1:g.45931936_45931937delinsAC	GRCh37
NC_000011.8:g.45888512_45888513delinsAC	NCBI36
NG_008460.1:g.12738_12739delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.953-74_953-73delinsGT MANE Select	ENSP00000368024.5:n.953-74_953-73delinsGT
ENST00000241041.7:c.953-209_953-208delinsGT	ENSP00000241041.3:n.953-209_953-208delinsGT
ENST00000378750.9:c.953-74_953-73delinsGT	ENSP00000368024.5:n.953-74_953-73delinsGT
ENST00000523721.2:n.183-74_183-73delinsGT
ENST00000532681.5:c.668-74_668-73delinsGT	ENSP00000434654.1:n.668-74_668-73delinsGT
NM_004813.2:c.953-74_953-73delinsGT	NP_004804.1:n.953-74_953-73delinsGT
NM_057174.2:c.953-209_953-208delinsGT	NP_476515.1:n.953-209_953-208delinsGT
XM_011520474.1:c.830-74_830-73delinsGT	XP_011518776.1:n.830-74_830-73delinsGT
NM_004813.3:c.953-74_953-73delinsGT	NP_004804.1:n.953-74_953-73delinsGT
NM_004813.4:c.953-74_953-73delinsGT MANE Select	NP_004804.2:n.953-74_953-73delinsGT
NM_057174.3:c.953-209_953-208delinsGT	NP_476515.2:n.953-209_953-208delinsGT