Canonical Allele Identifier: CA364155707
Gene: PEX6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42969728G>A , CM000668.2:g.42969728G>A GRCh38
NC_000006.11:g.42937466G>A , CM000668.1:g.42937466G>A GRCh37
NC_000006.10:g.43045444G>A NCBI36
NG_008370.1:g.14516C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000304611.13:c.1307C>T MANE Select ENSP00000303511.8:p.Pro436Leu
ENST00000244546.4:c.1307C>T ENSP00000244546.4:p.Pro436Leu
ENST00000304611.12:c.1307C>T ENSP00000303511.8:p.Pro436Leu
NM_000287.3:c.1307C>T NP_000278.3:p.Pro436Leu
NM_001316313.1:c.1043C>T NP_001303242.1:p.Pro348Leu
NR_133009.1:n.1400C>T
XM_011514661.1:c.1223C>T XP_011512963.1:p.Pro408Leu
XR_926246.1:n.1400C>T
XM_011514661.2:c.1223C>T XP_011512963.1:p.Pro408Leu
XR_001743466.2:n.2381C>T
NM_000287.4:c.1307C>T MANE Select NP_000278.3:p.Pro436Leu
NM_001316313.2:c.1043C>T NP_001303242.1:p.Pro348Leu
NR_133009.2:n.1338C>T