Canonical Allele Identifier: CA1968698282

Gene: PEX16

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910360_45910361delinsAC , CM000673.2:g.45910360_45910361delinsAC	GRCh38
NC_000011.9:g.45931911_45931912delinsAC , CM000673.1:g.45931911_45931912delinsAC	GRCh37
NC_000011.8:g.45888487_45888488delinsAC	NCBI36
NG_008460.1:g.12763_12764delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.953-49_953-48delinsGT MANE Select	ENSP00000368024.5:n.953-49_953-48delinsGT
ENST00000241041.7:c.953-184_953-183delinsGT	ENSP00000241041.3:n.953-184_953-183delinsGT
ENST00000378750.9:c.953-49_953-48delinsGT	ENSP00000368024.5:n.953-49_953-48delinsGT
ENST00000523721.2:n.183-49_183-48delinsGT
ENST00000532681.5:c.668-49_668-48delinsGT	ENSP00000434654.1:n.668-49_668-48delinsGT
NM_004813.2:c.953-49_953-48delinsGT	NP_004804.1:n.953-49_953-48delinsGT
NM_057174.2:c.953-184_953-183delinsGT	NP_476515.1:n.953-184_953-183delinsGT
XM_011520474.1:c.830-49_830-48delinsGT	XP_011518776.1:n.830-49_830-48delinsGT
NM_004813.3:c.953-49_953-48delinsGT	NP_004804.1:n.953-49_953-48delinsGT
NM_004813.4:c.953-49_953-48delinsGT MANE Select	NP_004804.2:n.953-49_953-48delinsGT
NM_057174.3:c.953-184_953-183delinsGT	NP_476515.2:n.953-184_953-183delinsGT