Canonical Allele Identifier: CA2791291477

Gene: PEX16

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910393_45910394insT , CM000673.2:g.45910393_45910394insT	GRCh38
NC_000011.9:g.45931944_45931945insT , CM000673.1:g.45931944_45931945insT	GRCh37
NC_000011.8:g.45888520_45888521insT	NCBI36
NG_008460.1:g.12730_12731insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.953-82_953-81insA MANE Select	ENSP00000368024.5:n.953-82_953-81insA
ENST00000241041.7:c.953-217_953-216insA	ENSP00000241041.3:n.953-217_953-216insA
ENST00000378750.9:c.953-82_953-81insA	ENSP00000368024.5:n.953-82_953-81insA
ENST00000523721.2:n.183-82_183-81insA
ENST00000532681.5:c.668-82_668-81insA	ENSP00000434654.1:n.668-82_668-81insA
NM_004813.2:c.953-82_953-81insA	NP_004804.1:n.953-82_953-81insA
NM_057174.2:c.953-217_953-216insA	NP_476515.1:n.953-217_953-216insA
XM_011520474.1:c.830-82_830-81insA	XP_011518776.1:n.830-82_830-81insA
NM_004813.3:c.953-82_953-81insA	NP_004804.1:n.953-82_953-81insA
NM_004813.4:c.953-82_953-81insA MANE Select	NP_004804.2:n.953-82_953-81insA
NM_057174.3:c.953-217_953-216insA	NP_476515.2:n.953-217_953-216insA