Canonical Allele Identifier: CA2791291455
Gene: PEX16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45910376C>A , CM000673.2:g.45910376C>A GRCh38
NC_000011.9:g.45931927C>A , CM000673.1:g.45931927C>A GRCh37
NC_000011.8:g.45888503C>A NCBI36
NG_008460.1:g.12748G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378750.10:c.953-64G>T MANE Select ENSP00000368024.5:n.953-64G>T
ENST00000241041.7:c.953-199G>T ENSP00000241041.3:n.953-199G>T
ENST00000378750.9:c.953-64G>T ENSP00000368024.5:n.953-64G>T
ENST00000523721.2:n.183-64G>T
ENST00000532681.5:c.668-64G>T ENSP00000434654.1:n.668-64G>T
NM_004813.2:c.953-64G>T NP_004804.1:n.953-64G>T
NM_057174.2:c.953-199G>T NP_476515.1:n.953-199G>T
XM_011520474.1:c.830-64G>T XP_011518776.1:n.830-64G>T
NM_004813.3:c.953-64G>T NP_004804.1:n.953-64G>T
NM_004813.4:c.953-64G>T MANE Select NP_004804.2:n.953-64G>T
NM_057174.3:c.953-199G>T NP_476515.2:n.953-199G>T