Canonical Allele Identifier: CA210645

Gene: PEX6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42966813G>A , CM000668.2:g.42966813G>A	GRCh38
NC_000006.11:g.42934551G>A , CM000668.1:g.42934551G>A	GRCh37
NC_000006.10:g.43042529G>A	NCBI36
NG_008370.1:g.17431C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000287.4:c.1930C>T MANE Select	NP_000278.3:p.Arg644Trp
ENST00000304611.13:c.1930C>T MANE Select	ENSP00000303511.8:p.Arg644Trp
NM_000287.3:c.1930C>T	NP_000278.3:p.Arg644Trp
NM_001316313.1:c.1666C>T	NP_001303242.1:p.Arg556Trp
NM_001316313.2:c.1666C>T	NP_001303242.1:p.Arg556Trp
NR_133009.1:n.2023C>T
NR_133009.2:n.1961C>T
ENST00000244546.4:c.1930C>T	ENSP00000244546.4:p.Arg644Trp
ENST00000304611.12:c.1930C>T	ENSP00000303511.8:p.Arg644Trp
XM_011514661.1:c.1846C>T	XP_011512963.1:p.Arg616Trp
XM_011514661.2:c.1846C>T	XP_011512963.1:p.Arg616Trp
XR_001743466.2:n.2892C>T
XR_926246.1:n.1911C>T