Canonical Allele Identifier: CA380223038
Gene: PEX16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.45931722T>G (hg19) chr11:g.45910171T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45910171T>G , CM000673.2:g.45910171T>G GRCh38
NC_000011.9:g.45931722T>G , CM000673.1:g.45931722T>G GRCh37
NC_000011.8:g.45888298T>G NCBI36
NG_008460.1:g.12953A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378750.10:c.*83A>C MANE Select ENSP00000368024.5:n.*83A>C
ENST00000241041.7:c.959A>C ENSP00000241041.3:p.Gln320Pro
ENST00000523721.2:n.324A>C
NM_004813.2:c.*83A>C NP_004804.1:n.*83A>C
NM_057174.2:c.959A>C NP_476515.1:p.Gln320Pro
NM_004813.3:c.*83A>C NP_004804.1:n.*83A>C
NM_004813.4:c.*83A>C MANE Select NP_004804.2:n.*83A>C
NM_057174.3:c.959A>C NP_476515.2:p.Gln320Pro
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