Canonical Allele Identifier: CA138237421
Community Standard Title: NM_000287.4(PEX6):c.882+1G>A
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42978268C>T , CM000668.2:g.42978268C>T GRCh38
NC_000006.11:g.42946006C>T , CM000668.1:g.42946006C>T GRCh37
NC_000006.10:g.43053984C>T NCBI36
NG_008370.1:g.5976G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000287.4:c.882+1G>A MANE Select NP_000278.3:n.882+1G>A
ENST00000304611.13:c.882+1G>A MANE Select ENSP00000303511.8:n.882+1G>A
NM_000287.3:c.882+1G>A NP_000278.3:n.882+1G>A
NM_001316313.1:c.618+265G>A NP_001303242.1:n.618+265G>A
NM_001316313.2:c.618+265G>A NP_001303242.1:n.618+265G>A
NR_133009.1:n.975+1G>A
NR_133009.2:n.913+1G>A
ENST00000244546.4:c.882+1G>A ENSP00000244546.4:n.882+1G>A
ENST00000304611.12:c.882+1G>A ENSP00000303511.8:n.882+1G>A
XM_011514661.1:c.882+1G>A XP_011512963.1:n.882+1G>A
XM_011514661.2:c.882+1G>A XP_011512963.1:n.882+1G>A
XR_001743466.2:n.1956+1G>A
XR_926246.1:n.975+1G>A