Canonical Allele Identifier: CA2773213633

Gene: PEX7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136866800_136866801insAGA , CM000668.2:g.136866800_136866801insAGA	GRCh38
NC_000006.11:g.137187938_137187939insAGA , CM000668.1:g.137187938_137187939insAGA	GRCh37
NC_000006.10:g.137229631_137229632insAGA	NCBI36
NG_008462.1:g.49221_49222insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.633+67_633+68insAGA MANE Select	ENSP00000315680.3:n.633+67_633+68insAGA
ENST00000541292.6:c.633+67_633+68insAGA	ENSP00000441004.1:n.633+67_633+68insAGA
ENST00000678002.1:c.321+67_321+68insAGA
ENST00000678557.1:c.519+67_519+68insAGA	ENSP00000502962.1:n.519+67_519+68insAGA
ENST00000678593.1:c.638+67_638+68insAGA	ENSP00000503841.1:n.638+67_638+68insAGA
ENST00000679286.1:c.513+67_513+68insAGA	ENSP00000503168.1:n.513+67_513+68insAGA
ENST00000318471.4:c.633+67_633+68insAGA	ENSP00000315680.3:n.633+67_633+68insAGA
ENST00000541292.5:c.633+67_633+68insAGA	ENSP00000441004.1:n.633+67_633+68insAGA
NM_000288.3:c.633+67_633+68insAGA	NP_000279.1:n.633+67_633+68insAGA
XM_005267019.3:c.519+67_519+68insAGA	XP_005267076.1:n.519+67_519+68insAGA
XM_006715502.1:c.340-3090_340-3089insAGA	XP_006715565.1:n.340-3090_340-3089insAGA
XM_011535900.1:c.526+20619_526+20620insAGA	XP_011534202.1:n.526+20619_526+20620insAGA
XM_005267019.4:c.519+67_519+68insAGA	XP_005267076.1:n.519+67_519+68insAGA
XM_006715502.2:c.340-3090_340-3089insAGA	XP_006715565.1:n.340-3090_340-3089insAGA
XM_017010934.2:c.526+20619_526+20620insAGA	XP_016866423.1:n.526+20619_526+20620insAGA
NM_000288.4:c.633+67_633+68insAGA MANE Select	NP_000279.1:n.633+67_633+68insAGA