Canonical Allele Identifier: CA2791291464

Gene: PEX16

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910386_45910387insACT , CM000673.2:g.45910386_45910387insACT	GRCh38
NC_000011.9:g.45931937_45931938insACT , CM000673.1:g.45931937_45931938insACT	GRCh37
NC_000011.8:g.45888513_45888514insACT	NCBI36
NG_008460.1:g.12737_12738insAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.953-75_953-74insAGT MANE Select	ENSP00000368024.5:n.953-75_953-74insAGT
ENST00000241041.7:c.953-210_953-209insAGT	ENSP00000241041.3:n.953-210_953-209insAGT
ENST00000378750.9:c.953-75_953-74insAGT	ENSP00000368024.5:n.953-75_953-74insAGT
ENST00000523721.2:n.183-75_183-74insAGT
ENST00000532681.5:c.668-75_668-74insAGT	ENSP00000434654.1:n.668-75_668-74insAGT
NM_004813.2:c.953-75_953-74insAGT	NP_004804.1:n.953-75_953-74insAGT
NM_057174.2:c.953-210_953-209insAGT	NP_476515.1:n.953-210_953-209insAGT
XM_011520474.1:c.830-75_830-74insAGT	XP_011518776.1:n.830-75_830-74insAGT
NM_004813.3:c.953-75_953-74insAGT	NP_004804.1:n.953-75_953-74insAGT
NM_004813.4:c.953-75_953-74insAGT MANE Select	NP_004804.2:n.953-75_953-74insAGT
NM_057174.3:c.953-210_953-209insAGT	NP_476515.2:n.953-210_953-209insAGT