Canonical Allele Identifier: CA2791291462

Gene: PEX16

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910382_45910383insAG , CM000673.2:g.45910382_45910383insAG	GRCh38
NC_000011.9:g.45931933_45931934insAG , CM000673.1:g.45931933_45931934insAG	GRCh37
NC_000011.8:g.45888509_45888510insAG	NCBI36
NG_008460.1:g.12741_12742insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.953-71_953-70insCT MANE Select	ENSP00000368024.5:n.953-71_953-70insCT
ENST00000241041.7:c.953-206_953-205insCT	ENSP00000241041.3:n.953-206_953-205insCT
ENST00000378750.9:c.953-71_953-70insCT	ENSP00000368024.5:n.953-71_953-70insCT
ENST00000523721.2:n.183-71_183-70insCT
ENST00000532681.5:c.668-71_668-70insCT	ENSP00000434654.1:n.668-71_668-70insCT
NM_004813.2:c.953-71_953-70insCT	NP_004804.1:n.953-71_953-70insCT
NM_057174.2:c.953-206_953-205insCT	NP_476515.1:n.953-206_953-205insCT
XM_011520474.1:c.830-71_830-70insCT	XP_011518776.1:n.830-71_830-70insCT
NM_004813.3:c.953-71_953-70insCT	NP_004804.1:n.953-71_953-70insCT
NM_004813.4:c.953-71_953-70insCT MANE Select	NP_004804.2:n.953-71_953-70insCT
NM_057174.3:c.953-206_953-205insCT	NP_476515.2:n.953-206_953-205insCT