Canonical Allele Identifier: CA2680489817

Gene: PEX7

Linked Data

• ClinVar Variation Id: 2863692
• ClinVar RCV Id: RCV003653870
• gnomAD v4: 6-136866747-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136866748del , CM000668.2:g.136866748del	GRCh38
NC_000006.11:g.137187886del , CM000668.1:g.137187886del	GRCh37
NC_000006.10:g.137229579del	NCBI36
NG_008462.1:g.49169del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.633+15del MANE Select	ENSP00000315680.3:n.633+15del
ENST00000541292.6:c.633+15del	ENSP00000441004.1:n.633+15del
ENST00000678002.1:c.321+15del
ENST00000678557.1:c.519+15del	ENSP00000502962.1:n.519+15del
ENST00000678593.1:c.638+15del	ENSP00000503841.1:n.638+15del
ENST00000679286.1:c.513+15del	ENSP00000503168.1:n.513+15del
ENST00000318471.4:c.633+15del	ENSP00000315680.3:n.633+15del
ENST00000541292.5:c.633+15del	ENSP00000441004.1:n.633+15del
NM_000288.3:c.633+15del	NP_000279.1:n.633+15del
XM_005267019.3:c.519+15del	XP_005267076.1:n.519+15del
XM_006715502.1:c.340-3142del	XP_006715565.1:n.340-3142del
XM_011535900.1:c.526+20567del	XP_011534202.1:n.526+20567del
XM_005267019.4:c.519+15del	XP_005267076.1:n.519+15del
XM_006715502.2:c.340-3142del	XP_006715565.1:n.340-3142del
XM_017010934.2:c.526+20567del	XP_016866423.1:n.526+20567del
NM_000288.4:c.633+15del MANE Select	NP_000279.1:n.633+15del