Canonical Allele Identifier: CA1624312453

Gene: PEX6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42969606T= , CM000668.2:g.42969606T=	GRCh38
NC_000006.11:g.42937344T= , CM000668.1:g.42937344T=	GRCh37
NC_000006.10:g.43045322T=	NCBI36
NG_008370.1:g.14638A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304611.13:c.1367+62A= MANE Select	ENSP00000303511.8:n.1367+62A=
ENST00000244546.4:c.1367+62A=	ENSP00000244546.4:n.1367+62A=
ENST00000304611.12:c.1367+62A=	ENSP00000303511.8:n.1367+62A=
NM_000287.3:c.1367+62A=	NP_000278.3:n.1367+62A=
NM_001316313.1:c.1103+62A=	NP_001303242.1:n.1103+62A=
NR_133009.1:n.1460+62A=
XM_011514661.1:c.1283+62A=	XP_011512963.1:n.1283+62A=
XR_926246.1:n.1460+62A=
XM_011514661.2:c.1283+62A=	XP_011512963.1:n.1283+62A=
XR_001743466.2:n.2441+62A=
NM_000287.4:c.1367+62A= MANE Select	NP_000278.3:n.1367+62A=
NM_001316313.2:c.1103+62A=	NP_001303242.1:n.1103+62A=
NR_133009.2:n.1398+62A=