Canonical Allele Identifier: CA364159321
Community Standard Title: NM_000287.4(PEX6):c.1046+1G>T
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42974874C>A , CM000668.2:g.42974874C>A GRCh38
NC_000006.11:g.42942612C>A , CM000668.1:g.42942612C>A GRCh37
NC_000006.10:g.43050590C>A NCBI36
NG_008370.1:g.9370G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000287.4:c.1046+1G>T MANE Select NP_000278.3:n.1046+1G>T
ENST00000304611.13:c.1046+1G>T MANE Select ENSP00000303511.8:n.1046+1G>T
NM_000287.3:c.1046+1G>T NP_000278.3:n.1046+1G>T
NM_001316313.1:c.782+1G>T NP_001303242.1:n.782+1G>T
NM_001316313.2:c.782+1G>T NP_001303242.1:n.782+1G>T
NR_133009.1:n.1139+1G>T
NR_133009.2:n.1077+1G>T
ENST00000244546.4:c.1046+1G>T ENSP00000244546.4:n.1046+1G>T
ENST00000304611.12:c.1046+1G>T ENSP00000303511.8:n.1046+1G>T
XM_011514661.1:c.1046+1G>T XP_011512963.1:n.1046+1G>T
XM_011514661.2:c.1046+1G>T XP_011512963.1:n.1046+1G>T
XR_001743466.2:n.2120+1G>T
XR_926246.1:n.1139+1G>T