Canonical Allele Identifier: CA2678796826
Gene: PEX6 HGNC NCBI

Linked Data

gnomAD v4: 6-42969814-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42969814A>T , CM000668.2:g.42969814A>T GRCh38
NC_000006.11:g.42937552A>T , CM000668.1:g.42937552A>T GRCh37
NC_000006.10:g.43045530A>T NCBI36
NG_008370.1:g.14430T>A

Transcript Alleles

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