Canonical Allele Identifier: CA2791291467

Gene: PEX16

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910387_45910388insAGA , CM000673.2:g.45910387_45910388insAGA	GRCh38
NC_000011.9:g.45931938_45931939insAGA , CM000673.1:g.45931938_45931939insAGA	GRCh37
NC_000011.8:g.45888514_45888515insAGA	NCBI36
NG_008460.1:g.12736_12737insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.953-76_953-75insTCT MANE Select	ENSP00000368024.5:n.953-76_953-75insTCT
ENST00000241041.7:c.953-211_953-210insTCT	ENSP00000241041.3:n.953-211_953-210insTCT
ENST00000378750.9:c.953-76_953-75insTCT	ENSP00000368024.5:n.953-76_953-75insTCT
ENST00000523721.2:n.183-76_183-75insTCT
ENST00000532681.5:c.668-76_668-75insTCT	ENSP00000434654.1:n.668-76_668-75insTCT
NM_004813.2:c.953-76_953-75insTCT	NP_004804.1:n.953-76_953-75insTCT
NM_057174.2:c.953-211_953-210insTCT	NP_476515.1:n.953-211_953-210insTCT
XM_011520474.1:c.830-76_830-75insTCT	XP_011518776.1:n.830-76_830-75insTCT
NM_004813.3:c.953-76_953-75insTCT	NP_004804.1:n.953-76_953-75insTCT
NM_004813.4:c.953-76_953-75insTCT MANE Select	NP_004804.2:n.953-76_953-75insTCT
NM_057174.3:c.953-211_953-210insTCT	NP_476515.2:n.953-211_953-210insTCT