Canonical Allele Identifier: CA364152231
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42966306G>A , CM000668.2:g.42966306G>A GRCh38
NC_000006.11:g.42934044G>A , CM000668.1:g.42934044G>A GRCh37
NC_000006.10:g.43042022G>A NCBI36
NG_008370.1:g.17938C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000287.4:c.2236C>T MANE Select NP_000278.3:p.Pro746Ser
ENST00000304611.13:c.2236C>T MANE Select ENSP00000303511.8:p.Pro746Ser
NM_000287.3:c.2236C>T NP_000278.3:p.Pro746Ser
NM_001316313.1:c.1972C>T NP_001303242.1:p.Pro658Ser
NM_001316313.2:c.1972C>T NP_001303242.1:p.Pro658Ser
NR_133009.1:n.2208+198C>T
NR_133009.2:n.2146+198C>T
ENST00000244546.4:c.2115+198C>T ENSP00000244546.4:n.2115+198C>T
ENST00000304611.12:c.2236C>T ENSP00000303511.8:p.Pro746Ser
XM_011514661.1:c.2152C>T XP_011512963.1:p.Pro718Ser
XM_011514661.2:c.2152C>T XP_011512963.1:p.Pro718Ser
XR_001743466.2:n.3198C>T