Canonical Allele Identifier: CA1968698124
Gene: PEX16 HGNC NCBI

Linked Data

dbSNP Id: rs2086758987

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45910057G>A , CM000673.2:g.45910057G>A GRCh38
NC_000011.9:g.45931608G>A , CM000673.1:g.45931608G>A GRCh37
NC_000011.8:g.45888184G>A NCBI36
NG_008460.1:g.13067C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378750.10:c.*197C>T MANE Select ENSP00000368024.5:n.*197C>T
ENST00000241041.7:c.*32C>T ENSP00000241041.3:n.*32C>T
NM_004813.2:c.*197C>T NP_004804.1:n.*197C>T
NM_057174.2:c.*32C>T NP_476515.1:n.*32C>T
NM_004813.3:c.*197C>T NP_004804.1:n.*197C>T
NM_004813.4:c.*197C>T MANE Select NP_004804.2:n.*197C>T
NM_057174.3:c.*32C>T NP_476515.2:n.*32C>T