Canonical Allele Identifier: CA1624312466

Gene: PEX6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42969621G= , CM000668.2:g.42969621G=	GRCh38
NC_000006.11:g.42937359G= , CM000668.1:g.42937359G=	GRCh37
NC_000006.10:g.43045337G=	NCBI36
NG_008370.1:g.14623C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304611.13:c.1367+47C= MANE Select	ENSP00000303511.8:n.1367+47C=
ENST00000244546.4:c.1367+47C=	ENSP00000244546.4:n.1367+47C=
ENST00000304611.12:c.1367+47C=	ENSP00000303511.8:n.1367+47C=
NM_000287.3:c.1367+47C=	NP_000278.3:n.1367+47C=
NM_001316313.1:c.1103+47C=	NP_001303242.1:n.1103+47C=
NR_133009.1:n.1460+47C=
XM_011514661.1:c.1283+47C=	XP_011512963.1:n.1283+47C=
XR_926246.1:n.1460+47C=
XM_011514661.2:c.1283+47C=	XP_011512963.1:n.1283+47C=
XR_001743466.2:n.2441+47C=
NM_000287.4:c.1367+47C= MANE Select	NP_000278.3:n.1367+47C=
NM_001316313.2:c.1103+47C=	NP_001303242.1:n.1103+47C=
NR_133009.2:n.1398+47C=