Canonical Allele Identifier: CA1624312842
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42969827G= , CM000668.2:g.42969827G= GRCh38
NC_000006.11:g.42937565G= , CM000668.1:g.42937565G= GRCh37
NC_000006.10:g.43045543G= NCBI36
NG_008370.1:g.14417C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304611.13:c.1234-26C= MANE Select ENSP00000303511.8:n.1234-26C=
ENST00000244546.4:c.1234-26C= ENSP00000244546.4:n.1234-26C=
ENST00000304611.12:c.1234-26C= ENSP00000303511.8:n.1234-26C=
NM_000287.3:c.1234-26C= NP_000278.3:n.1234-26C=
NM_001316313.1:c.970-26C= NP_001303242.1:n.970-26C=
NR_133009.1:n.1327-26C=
XM_011514661.1:c.1150-26C= XP_011512963.1:n.1150-26C=
XR_926246.1:n.1327-26C=
XM_011514661.2:c.1150-26C= XP_011512963.1:n.1150-26C=
XR_001743466.2:n.2308-26C=
NM_000287.4:c.1234-26C= MANE Select NP_000278.3:n.1234-26C=
NM_001316313.2:c.970-26C= NP_001303242.1:n.970-26C=
NR_133009.2:n.1265-26C=