Canonical Allele Identifier: CA1968698255

Gene: PEX16

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910304T= , CM000673.2:g.45910304T=	GRCh38
NC_000011.9:g.45931855T= , CM000673.1:g.45931855T=	GRCh37
NC_000011.8:g.45888431T=	NCBI36
NG_008460.1:g.12820A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.961A= MANE Select	ENSP00000368024.5:p.Met321=
ENST00000241041.7:c.953-127A=	ENSP00000241041.3:n.953-127A=
ENST00000378750.9:c.961A=	ENSP00000368024.5:p.Met321=
ENST00000523721.2:n.191A=
ENST00000532681.5:c.676A=	ENSP00000434654.1:p.Met226=
NM_004813.2:c.961A=	NP_004804.1:p.Met321=
NM_057174.2:c.953-127A=	NP_476515.1:n.953-127A=
XM_011520474.1:c.838A=	XP_011518776.1:p.Met280=
NM_004813.3:c.961A=	NP_004804.1:p.Met321=
NM_004813.4:c.961A= MANE Select	NP_004804.2:p.Met321=
NM_057174.3:c.953-127A=	NP_476515.2:n.953-127A=