Canonical Allele Identifier: CA2791291473

Gene: PEX16

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910391_45910400del , CM000673.2:g.45910391_45910400del	GRCh38
NC_000011.9:g.45931942_45931951del , CM000673.1:g.45931942_45931951del	GRCh37
NC_000011.8:g.45888518_45888527del	NCBI36
NG_008460.1:g.12724_12733del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.953-88_953-79del MANE Select	ENSP00000368024.5:n.953-88_953-79del
ENST00000241041.7:c.953-223_953-214del	ENSP00000241041.3:n.953-223_953-214del
ENST00000378750.9:c.953-88_953-79del	ENSP00000368024.5:n.953-88_953-79del
ENST00000523721.2:n.183-88_183-79del
ENST00000532681.5:c.668-88_668-79del	ENSP00000434654.1:n.668-88_668-79del
NM_004813.2:c.953-88_953-79del	NP_004804.1:n.953-88_953-79del
NM_057174.2:c.953-223_953-214del	NP_476515.1:n.953-223_953-214del
XM_011520474.1:c.830-88_830-79del	XP_011518776.1:n.830-88_830-79del
NM_004813.3:c.953-88_953-79del	NP_004804.1:n.953-88_953-79del
NM_004813.4:c.953-88_953-79del MANE Select	NP_004804.2:n.953-88_953-79del
NM_057174.3:c.953-223_953-214del	NP_476515.2:n.953-223_953-214del