Canonical Allele Identifier: CA1968698287

Gene: PEX16

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910370_45910374delinsCACAT , CM000673.2:g.45910370_45910374delinsCACAT	GRCh38
NC_000011.9:g.45931921_45931925delinsCACAT , CM000673.1:g.45931921_45931925delinsCACAT	GRCh37
NC_000011.8:g.45888497_45888501delinsCACAT	NCBI36
NG_008460.1:g.12750_12754delinsATGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.953-62_953-58delinsATGTG MANE Select	ENSP00000368024.5:n.953-62_953-58delinsATGTG
ENST00000241041.7:c.953-197_953-193delinsATGTG	ENSP00000241041.3:n.953-197_953-193delinsATGTG
ENST00000378750.9:c.953-62_953-58delinsATGTG	ENSP00000368024.5:n.953-62_953-58delinsATGTG
ENST00000523721.2:n.183-62_183-58delinsATGTG
ENST00000532681.5:c.668-62_668-58delinsATGTG	ENSP00000434654.1:n.668-62_668-58delinsATGTG
NM_004813.2:c.953-62_953-58delinsATGTG	NP_004804.1:n.953-62_953-58delinsATGTG
NM_057174.2:c.953-197_953-193delinsATGTG	NP_476515.1:n.953-197_953-193delinsATGTG
XM_011520474.1:c.830-62_830-58delinsATGTG	XP_011518776.1:n.830-62_830-58delinsATGTG
NM_004813.3:c.953-62_953-58delinsATGTG	NP_004804.1:n.953-62_953-58delinsATGTG
NM_004813.4:c.953-62_953-58delinsATGTG MANE Select	NP_004804.2:n.953-62_953-58delinsATGTG
NM_057174.3:c.953-197_953-193delinsATGTG	NP_476515.2:n.953-197_953-193delinsATGTG