Canonical Allele Identifier: CA1624312775

Gene: PEX6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42969797C= , CM000668.2:g.42969797C=	GRCh38
NC_000006.11:g.42937535C= , CM000668.1:g.42937535C=	GRCh37
NC_000006.10:g.43045513C=	NCBI36
NG_008370.1:g.14447G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304611.13:c.1238G= MANE Select	ENSP00000303511.8:p.Gly413=
ENST00000244546.4:c.1238G=	ENSP00000244546.4:p.Gly413=
ENST00000304611.12:c.1238G=	ENSP00000303511.8:p.Gly413=
NM_000287.3:c.1238G=	NP_000278.3:p.Gly413=
NM_001316313.1:c.974G=	NP_001303242.1:p.Gly325=
NR_133009.1:n.1331G=
XM_011514661.1:c.1154G=	XP_011512963.1:p.Gly385=
XR_926246.1:n.1331G=
XM_011514661.2:c.1154G=	XP_011512963.1:p.Gly385=
XR_001743466.2:n.2312G=
NM_000287.4:c.1238G= MANE Select	NP_000278.3:p.Gly413=
NM_001316313.2:c.974G=	NP_001303242.1:p.Gly325=
NR_133009.2:n.1269G=