Canonical Allele Identifier: CA2770830032

Gene: PEX6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42969816_42969817insGTG , CM000668.2:g.42969816_42969817insGTG	GRCh38
NC_000006.11:g.42937554_42937555insGTG , CM000668.1:g.42937554_42937555insGTG	GRCh37
NC_000006.10:g.43045532_43045533insGTG	NCBI36
NG_008370.1:g.14427_14428insCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304611.13:c.1234-16_1234-15insCAC MANE Select	ENSP00000303511.8:n.1234-16_1234-15insCAC
ENST00000244546.4:c.1234-16_1234-15insCAC	ENSP00000244546.4:n.1234-16_1234-15insCAC
ENST00000304611.12:c.1234-16_1234-15insCAC	ENSP00000303511.8:n.1234-16_1234-15insCAC
NM_000287.3:c.1234-16_1234-15insCAC	NP_000278.3:n.1234-16_1234-15insCAC
NM_001316313.1:c.970-16_970-15insCAC	NP_001303242.1:n.970-16_970-15insCAC
NR_133009.1:n.1327-16_1327-15insCAC
XM_011514661.1:c.1150-16_1150-15insCAC	XP_011512963.1:n.1150-16_1150-15insCAC
XR_926246.1:n.1327-16_1327-15insCAC
XM_011514661.2:c.1150-16_1150-15insCAC	XP_011512963.1:n.1150-16_1150-15insCAC
XR_001743466.2:n.2308-16_2308-15insCAC
NM_000287.4:c.1234-16_1234-15insCAC MANE Select	NP_000278.3:n.1234-16_1234-15insCAC
NM_001316313.2:c.970-16_970-15insCAC	NP_001303242.1:n.970-16_970-15insCAC
NR_133009.2:n.1265-16_1265-15insCAC