Canonical Allele Identifier: CA2845783231

Gene: PEX6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42969837_42969838insGT , CM000668.2:g.42969837_42969838insGT	GRCh38
NC_000006.11:g.42937575_42937576insGT , CM000668.1:g.42937575_42937576insGT	GRCh37
NC_000006.10:g.43045553_43045554insGT	NCBI36
NG_008370.1:g.14406_14407insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304611.13:c.1234-37_1234-36insAC MANE Select	ENSP00000303511.8:n.1234-37_1234-36insAC
ENST00000244546.4:c.1234-37_1234-36insAC	ENSP00000244546.4:n.1234-37_1234-36insAC
ENST00000304611.12:c.1234-37_1234-36insAC	ENSP00000303511.8:n.1234-37_1234-36insAC
NM_000287.3:c.1234-37_1234-36insAC	NP_000278.3:n.1234-37_1234-36insAC
NM_001316313.1:c.970-37_970-36insAC	NP_001303242.1:n.970-37_970-36insAC
NR_133009.1:n.1327-37_1327-36insAC
XM_011514661.1:c.1150-37_1150-36insAC	XP_011512963.1:n.1150-37_1150-36insAC
XR_926246.1:n.1327-37_1327-36insAC
XM_011514661.2:c.1150-37_1150-36insAC	XP_011512963.1:n.1150-37_1150-36insAC
XR_001743466.2:n.2308-37_2308-36insAC
NM_000287.4:c.1234-37_1234-36insAC MANE Select	NP_000278.3:n.1234-37_1234-36insAC
NM_001316313.2:c.970-37_970-36insAC	NP_001303242.1:n.970-37_970-36insAC
NR_133009.2:n.1265-37_1265-36insAC