Canonical Allele Identifier: CA2613278721

Gene: PEX16

Linked Data

• gnomAD v4: 11-45910381-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910381C>A , CM000673.2:g.45910381C>A	GRCh38
NC_000011.9:g.45931932C>A , CM000673.1:g.45931932C>A	GRCh37
NC_000011.8:g.45888508C>A	NCBI36
NG_008460.1:g.12743G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.953-69G>T MANE Select	ENSP00000368024.5:n.953-69G>T
ENST00000241041.7:c.953-204G>T	ENSP00000241041.3:n.953-204G>T
ENST00000378750.9:c.953-69G>T	ENSP00000368024.5:n.953-69G>T
ENST00000523721.2:n.183-69G>T
ENST00000532681.5:c.668-69G>T	ENSP00000434654.1:n.668-69G>T
NM_004813.2:c.953-69G>T	NP_004804.1:n.953-69G>T
NM_057174.2:c.953-204G>T	NP_476515.1:n.953-204G>T
XM_011520474.1:c.830-69G>T	XP_011518776.1:n.830-69G>T
NM_004813.3:c.953-69G>T	NP_004804.1:n.953-69G>T
NM_004813.4:c.953-69G>T MANE Select	NP_004804.2:n.953-69G>T
NM_057174.3:c.953-204G>T	NP_476515.2:n.953-204G>T