Canonical Allele Identifier: CA2773214696

Gene: PEX7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136872359_136872360insACG , CM000668.2:g.136872359_136872360insACG	GRCh38
NC_000006.11:g.137193497_137193498insACG , CM000668.1:g.137193497_137193498insACG	GRCh37
NC_000006.10:g.137235190_137235191insACG	NCBI36
NG_008462.1:g.54780_54781insACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.803+106_803+107insACG MANE Select	ENSP00000315680.3:n.803+106_803+107insACG
ENST00000541292.6:c.*68+106_*68+107insACG	ENSP00000441004.1:n.*68+106_*68+107insACG
ENST00000678002.1:c.491+106_491+107insACG
ENST00000678557.1:c.689+106_689+107insACG	ENSP00000502962.1:n.689+106_689+107insACG
ENST00000678593.1:c.914_915insACG	ENSP00000503841.1:n.914_915insACG
ENST00000679286.1:c.683+106_683+107insACG	ENSP00000503168.1:n.683+106_683+107insACG
ENST00000318471.4:c.803+106_803+107insACG	ENSP00000315680.3:n.803+106_803+107insACG
NM_000288.3:c.803+106_803+107insACG	NP_000279.1:n.803+106_803+107insACG
XM_005267019.3:c.689+106_689+107insACG	XP_005267076.1:n.689+106_689+107insACG
XM_006715502.1:c.509+106_509+107insACG	XP_006715565.1:n.509+106_509+107insACG
XM_011535900.1:c.527-25783_527-25782insACG	XP_011534202.1:n.527-25783_527-25782insACG
XM_005267019.4:c.689+106_689+107insACG	XP_005267076.1:n.689+106_689+107insACG
XM_006715502.2:c.509+106_509+107insACG	XP_006715565.1:n.509+106_509+107insACG
XM_017010934.2:c.527-25783_527-25782insACG	XP_016866423.1:n.527-25783_527-25782insACG
NM_000288.4:c.803+106_803+107insACG MANE Select	NP_000279.1:n.803+106_803+107insACG