Canonical Allele Identifier: CA2680489837

Gene: PEX7

Linked Data

• gnomAD v4: 6-136866802-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136866805dup , CM000668.2:g.136866805dup	GRCh38
NC_000006.11:g.137187943dup , CM000668.1:g.137187943dup	GRCh37
NC_000006.10:g.137229636dup	NCBI36
NG_008462.1:g.49226dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.633+72dup MANE Select	ENSP00000315680.3:n.633+72dup
ENST00000541292.6:c.633+72dup	ENSP00000441004.1:n.633+72dup
ENST00000678002.1:c.321+72dup
ENST00000678557.1:c.519+72dup	ENSP00000502962.1:n.519+72dup
ENST00000678593.1:c.638+72dup	ENSP00000503841.1:n.638+72dup
ENST00000679286.1:c.513+72dup	ENSP00000503168.1:n.513+72dup
ENST00000318471.4:c.633+72dup	ENSP00000315680.3:n.633+72dup
ENST00000541292.5:c.633+72dup	ENSP00000441004.1:n.633+72dup
NM_000288.3:c.633+72dup	NP_000279.1:n.633+72dup
XM_005267019.3:c.519+72dup	XP_005267076.1:n.519+72dup
XM_006715502.1:c.340-3085dup	XP_006715565.1:n.340-3085dup
XM_011535900.1:c.526+20624dup	XP_011534202.1:n.526+20624dup
XM_005267019.4:c.519+72dup	XP_005267076.1:n.519+72dup
XM_006715502.2:c.340-3085dup	XP_006715565.1:n.340-3085dup
XM_017010934.2:c.526+20624dup	XP_016866423.1:n.526+20624dup
NM_000288.4:c.633+72dup MANE Select	NP_000279.1:n.633+72dup