Canonical Allele Identifier: CA676924947

Gene: PEX16

Linked Data

• dbSNP Id: rs1287869236
• gnomAD v3: 11-45910389-C-A
• gnomAD v4: 11-45910389-C-A
• MyVariant Identifiers: chr11:g.45931940C>A (hg19) ; chr11:g.45910389C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45910389C>A , CM000673.2:g.45910389C>A	GRCh38
NC_000011.9:g.45931940C>A , CM000673.1:g.45931940C>A	GRCh37
NC_000011.8:g.45888516C>A	NCBI36
NG_008460.1:g.12735G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378750.10:c.953-77G>T MANE Select	ENSP00000368024.5:n.953-77G>T
ENST00000241041.7:c.953-212G>T	ENSP00000241041.3:n.953-212G>T
ENST00000378750.9:c.953-77G>T	ENSP00000368024.5:n.953-77G>T
ENST00000523721.2:n.183-77G>T
ENST00000532681.5:c.668-77G>T	ENSP00000434654.1:n.668-77G>T
NM_004813.2:c.953-77G>T	NP_004804.1:n.953-77G>T
NM_057174.2:c.953-212G>T	NP_476515.1:n.953-212G>T
XM_011520474.1:c.830-77G>T	XP_011518776.1:n.830-77G>T
NM_004813.3:c.953-77G>T	NP_004804.1:n.953-77G>T
NM_004813.4:c.953-77G>T MANE Select	NP_004804.2:n.953-77G>T
NM_057174.3:c.953-212G>T	NP_476515.2:n.953-212G>T