Canonical Allele Identifier: CA2680489136

Gene: PEX7

Linked Data

• gnomAD v4: 6-136826287-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136826294del , CM000668.2:g.136826294del	GRCh38
NC_000006.11:g.137147432del , CM000668.1:g.137147432del	GRCh37
NC_000006.10:g.137189125del	NCBI36
NG_008462.1:g.8715del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.189-25del MANE Select	ENSP00000315680.3:n.189-25del
ENST00000541292.6:c.189-25del	ENSP00000441004.1:n.189-25del
ENST00000678002.1:c.59-20del
ENST00000678557.1:c.75-25del	ENSP00000502962.1:n.75-25del
ENST00000678593.1:c.189-20del	ENSP00000503841.1:n.189-20del
ENST00000679286.1:c.69-25del	ENSP00000503168.1:n.69-25del
ENST00000318471.4:c.189-25del	ENSP00000315680.3:n.189-25del
ENST00000367756.8:c.189-25del	ENSP00000356730.4:n.189-25del
ENST00000541292.5:c.189-25del	ENSP00000441004.1:n.189-25del
NM_000288.3:c.189-25del	NP_000279.1:n.189-25del
XM_005267019.3:c.75-25del	XP_005267076.1:n.75-25del
XM_006715502.1:c.189-25del	XP_006715565.1:n.189-25del
XM_011535900.1:c.189-25del	XP_011534202.1:n.189-25del
XM_005267019.4:c.75-25del	XP_005267076.1:n.75-25del
XM_006715502.2:c.189-25del	XP_006715565.1:n.189-25del
XM_017010934.2:c.189-25del	XP_016866423.1:n.189-25del
NM_000288.4:c.189-25del MANE Select	NP_000279.1:n.189-25del