Canonical Allele Identifier: CA1624312833
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42969820A= , CM000668.2:g.42969820A= GRCh38
NC_000006.11:g.42937558A= , CM000668.1:g.42937558A= GRCh37
NC_000006.10:g.43045536A= NCBI36
NG_008370.1:g.14424T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304611.13:c.1234-19T= MANE Select ENSP00000303511.8:n.1234-19T=
ENST00000244546.4:c.1234-19T= ENSP00000244546.4:n.1234-19T=
ENST00000304611.12:c.1234-19T= ENSP00000303511.8:n.1234-19T=
NM_000287.3:c.1234-19T= NP_000278.3:n.1234-19T=
NM_001316313.1:c.970-19T= NP_001303242.1:n.970-19T=
NR_133009.1:n.1327-19T=
XM_011514661.1:c.1150-19T= XP_011512963.1:n.1150-19T=
XR_926246.1:n.1327-19T=
XM_011514661.2:c.1150-19T= XP_011512963.1:n.1150-19T=
XR_001743466.2:n.2308-19T=
NM_000287.4:c.1234-19T= MANE Select NP_000278.3:n.1234-19T=
NM_001316313.2:c.970-19T= NP_001303242.1:n.970-19T=
NR_133009.2:n.1265-19T=