Canonical Allele Identifier: CA2791291460

Gene: PEX16

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910380_45910381insGAG , CM000673.2:g.45910380_45910381insGAG	GRCh38
NC_000011.9:g.45931931_45931932insGAG , CM000673.1:g.45931931_45931932insGAG	GRCh37
NC_000011.8:g.45888507_45888508insGAG	NCBI36
NG_008460.1:g.12743_12744insCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.953-69_953-68insCTC MANE Select	ENSP00000368024.5:n.953-69_953-68insCTC
ENST00000241041.7:c.953-204_953-203insCTC	ENSP00000241041.3:n.953-204_953-203insCTC
ENST00000378750.9:c.953-69_953-68insCTC	ENSP00000368024.5:n.953-69_953-68insCTC
ENST00000523721.2:n.183-69_183-68insCTC
ENST00000532681.5:c.668-69_668-68insCTC	ENSP00000434654.1:n.668-69_668-68insCTC
NM_004813.2:c.953-69_953-68insCTC	NP_004804.1:n.953-69_953-68insCTC
NM_057174.2:c.953-204_953-203insCTC	NP_476515.1:n.953-204_953-203insCTC
XM_011520474.1:c.830-69_830-68insCTC	XP_011518776.1:n.830-69_830-68insCTC
NM_004813.3:c.953-69_953-68insCTC	NP_004804.1:n.953-69_953-68insCTC
NM_004813.4:c.953-69_953-68insCTC MANE Select	NP_004804.2:n.953-69_953-68insCTC
NM_057174.3:c.953-204_953-203insCTC	NP_476515.2:n.953-204_953-203insCTC