Canonical Allele Identifier: CA2791291469

Gene: PEX16

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910389_45910390insACA , CM000673.2:g.45910389_45910390insACA	GRCh38
NC_000011.9:g.45931940_45931941insACA , CM000673.1:g.45931940_45931941insACA	GRCh37
NC_000011.8:g.45888516_45888517insACA	NCBI36
NG_008460.1:g.12734_12735insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.953-78_953-77insTGT MANE Select	ENSP00000368024.5:n.953-78_953-77insTGT
ENST00000241041.7:c.953-213_953-212insTGT	ENSP00000241041.3:n.953-213_953-212insTGT
ENST00000378750.9:c.953-78_953-77insTGT	ENSP00000368024.5:n.953-78_953-77insTGT
ENST00000523721.2:n.183-78_183-77insTGT
ENST00000532681.5:c.668-78_668-77insTGT	ENSP00000434654.1:n.668-78_668-77insTGT
NM_004813.2:c.953-78_953-77insTGT	NP_004804.1:n.953-78_953-77insTGT
NM_057174.2:c.953-213_953-212insTGT	NP_476515.1:n.953-213_953-212insTGT
XM_011520474.1:c.830-78_830-77insTGT	XP_011518776.1:n.830-78_830-77insTGT
NM_004813.3:c.953-78_953-77insTGT	NP_004804.1:n.953-78_953-77insTGT
NM_004813.4:c.953-78_953-77insTGT MANE Select	NP_004804.2:n.953-78_953-77insTGT
NM_057174.3:c.953-213_953-212insTGT	NP_476515.2:n.953-213_953-212insTGT