Canonical Allele Identifier: CA1624312635

Gene: PEX6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42969717C= , CM000668.2:g.42969717C=	GRCh38
NC_000006.11:g.42937455C= , CM000668.1:g.42937455C=	GRCh37
NC_000006.10:g.43045433C=	NCBI36
NG_008370.1:g.14527G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304611.13:c.1318G= MANE Select	ENSP00000303511.8:p.Ala440=
ENST00000244546.4:c.1318G=	ENSP00000244546.4:p.Ala440=
ENST00000304611.12:c.1318G=	ENSP00000303511.8:p.Ala440=
NM_000287.3:c.1318G=	NP_000278.3:p.Ala440=
NM_001316313.1:c.1054G=	NP_001303242.1:p.Ala352=
NR_133009.1:n.1411G=
XM_011514661.1:c.1234G=	XP_011512963.1:p.Ala412=
XR_926246.1:n.1411G=
XM_011514661.2:c.1234G=	XP_011512963.1:p.Ala412=
XR_001743466.2:n.2392G=
NM_000287.4:c.1318G= MANE Select	NP_000278.3:p.Ala440=
NM_001316313.2:c.1054G=	NP_001303242.1:p.Ala352=
NR_133009.2:n.1349G=