Canonical Allele Identifier: CA364150527
Community Standard Title: NM_000287.4(PEX6):c.2667-2A>C
Gene: PEX6 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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