Canonical Allele Identifier: CA138221524
Community Standard Title: NM_000287.4(PEX6):c.2667-2A>G
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42964931T>C , CM000668.2:g.42964931T>C GRCh38
NC_000006.11:g.42932669T>C , CM000668.1:g.42932669T>C GRCh37
NC_000006.10:g.43040647T>C NCBI36
NG_008370.1:g.19313A>G
NG_008396.1:g.9170T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000287.4:c.2667-2A>G MANE Select NP_000278.3:n.2667-2A>G
ENST00000304611.13:c.2667-2A>G MANE Select ENSP00000303511.8:n.2667-2A>G
NM_000287.3:c.2667-2A>G NP_000278.3:n.2667-2A>G
NM_001316313.1:c.2403-2A>G NP_001303242.1:n.2403-2A>G
NM_001316313.2:c.2403-2A>G NP_001303242.1:n.2403-2A>G
NR_133009.1:n.2513-2A>G
NR_133009.2:n.2451-2A>G
ENST00000244546.4:c.2420-2A>G ENSP00000244546.4:n.2420-2A>G
ENST00000304611.12:c.2667-2A>G ENSP00000303511.8:n.2667-2A>G
XM_011514661.1:c.2583-2A>G XP_011512963.1:n.2583-2A>G
XM_011514661.2:c.2583-2A>G XP_011512963.1:n.2583-2A>G
XR_001743466.2:n.3629-2A>G