Canonical Allele Identifier: CA364153987
Community Standard Title: NM_000287.4(PEX6):c.1688+1G>T
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42968289C>A , CM000668.2:g.42968289C>A GRCh38
NC_000006.11:g.42936027C>A , CM000668.1:g.42936027C>A GRCh37
NC_000006.10:g.43044005C>A NCBI36
NG_008370.1:g.15955G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000287.4:c.1688+1G>T MANE Select NP_000278.3:n.1688+1G>T
ENST00000304611.13:c.1688+1G>T MANE Select ENSP00000303511.8:n.1688+1G>T
NM_000287.3:c.1688+1G>T NP_000278.3:n.1688+1G>T
NM_001316313.1:c.1424+1G>T NP_001303242.1:n.1424+1G>T
NM_001316313.2:c.1424+1G>T NP_001303242.1:n.1424+1G>T
NR_133009.1:n.1781+1G>T
NR_133009.2:n.1719+1G>T
ENST00000244546.4:c.1688+1G>T ENSP00000244546.4:n.1688+1G>T
ENST00000304611.12:c.1688+1G>T ENSP00000303511.8:n.1688+1G>T
XM_011514661.1:c.1604+1G>T XP_011512963.1:n.1604+1G>T
XM_011514661.2:c.1604+1G>T XP_011512963.1:n.1604+1G>T
XR_001743466.2:n.2650+1G>T
XR_926246.1:n.1669+1G>T