Canonical Allele Identifier: CA2678796808
Gene: PEX6 HGNC NCBI

Linked Data

gnomAD v4: 6-42969631-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42969631G>C , CM000668.2:g.42969631G>C GRCh38
NC_000006.11:g.42937369G>C , CM000668.1:g.42937369G>C GRCh37
NC_000006.10:g.43045347G>C NCBI36
NG_008370.1:g.14613C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000304611.13:c.1367+37C>G MANE Select ENSP00000303511.8:n.1367+37C>G
ENST00000244546.4:c.1367+37C>G ENSP00000244546.4:n.1367+37C>G
ENST00000304611.12:c.1367+37C>G ENSP00000303511.8:n.1367+37C>G
NM_000287.3:c.1367+37C>G NP_000278.3:n.1367+37C>G
NM_001316313.1:c.1103+37C>G NP_001303242.1:n.1103+37C>G
NR_133009.1:n.1460+37C>G
XM_011514661.1:c.1283+37C>G XP_011512963.1:n.1283+37C>G
XR_926246.1:n.1460+37C>G
XM_011514661.2:c.1283+37C>G XP_011512963.1:n.1283+37C>G
XR_001743466.2:n.2441+37C>G
NM_000287.4:c.1367+37C>G MANE Select NP_000278.3:n.1367+37C>G
NM_001316313.2:c.1103+37C>G NP_001303242.1:n.1103+37C>G
NR_133009.2:n.1398+37C>G