Canonical Allele Identifier: CA1624312554
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42969680C= , CM000668.2:g.42969680C= GRCh38
NC_000006.11:g.42937418C= , CM000668.1:g.42937418C= GRCh37
NC_000006.10:g.43045396C= NCBI36
NG_008370.1:g.14564G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304611.13:c.1355G= MANE Select ENSP00000303511.8:p.Arg452=
ENST00000244546.4:c.1355G= ENSP00000244546.4:p.Arg452=
ENST00000304611.12:c.1355G= ENSP00000303511.8:p.Arg452=
NM_000287.3:c.1355G= NP_000278.3:p.Arg452=
NM_001316313.1:c.1091G= NP_001303242.1:p.Arg364=
NR_133009.1:n.1448G=
XM_011514661.1:c.1271G= XP_011512963.1:p.Arg424=
XR_926246.1:n.1448G=
XM_011514661.2:c.1271G= XP_011512963.1:p.Arg424=
XR_001743466.2:n.2429G=
NM_000287.4:c.1355G= MANE Select NP_000278.3:p.Arg452=
NM_001316313.2:c.1091G= NP_001303242.1:p.Arg364=
NR_133009.2:n.1386G=