Canonical Allele Identifier: CA16512490
Gene: PEX11A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89682512T>C , CM000677.2:g.89682512T>C GRCh38
NC_000015.9:g.90225743T>C , CM000677.1:g.90225743T>C GRCh37
NC_000015.8:g.88026747T>C NCBI36
NG_029172.1:g.1906A>G

Transcript Alleles

HGVS Amino-acid Change
NM_003847.3:c.*865A>G MANE Select NP_003838.1:n.*865A>G
ENST00000300056.8:c.*865A>G MANE Select ENSP00000300056.3:n.*865A>G
NM_001271572.1:c.*865A>G NP_001258501.1:n.*865A>G
NM_001271572.2:c.*865A>G NP_001258501.1:n.*865A>G
NM_001271573.1:c.*865A>G NP_001258502.1:n.*865A>G
NM_001271573.2:c.*865A>G NP_001258502.1:n.*865A>G
NM_003847.2:c.*865A>G NP_003838.1:n.*865A>G
ENST00000300056.7:c.*865A>G ENSP00000300056.3:n.*865A>G
ENST00000557982.1:n.207-972A>G
ENST00000561224.5:c.173-972A>G ENSP00000453552.1:n.173-972A>G