Canonical Allele Identifier: CA2773213642

Gene: PEX7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136866804_136866805insAC , CM000668.2:g.136866804_136866805insAC	GRCh38
NC_000006.11:g.137187942_137187943insAC , CM000668.1:g.137187942_137187943insAC	GRCh37
NC_000006.10:g.137229635_137229636insAC	NCBI36
NG_008462.1:g.49225_49226insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.633+71_633+72insAC MANE Select	ENSP00000315680.3:n.633+71_633+72insAC
ENST00000541292.6:c.633+71_633+72insAC	ENSP00000441004.1:n.633+71_633+72insAC
ENST00000678002.1:c.321+71_321+72insAC
ENST00000678557.1:c.519+71_519+72insAC	ENSP00000502962.1:n.519+71_519+72insAC
ENST00000678593.1:c.638+71_638+72insAC	ENSP00000503841.1:n.638+71_638+72insAC
ENST00000679286.1:c.513+71_513+72insAC	ENSP00000503168.1:n.513+71_513+72insAC
ENST00000318471.4:c.633+71_633+72insAC	ENSP00000315680.3:n.633+71_633+72insAC
ENST00000541292.5:c.633+71_633+72insAC	ENSP00000441004.1:n.633+71_633+72insAC
NM_000288.3:c.633+71_633+72insAC	NP_000279.1:n.633+71_633+72insAC
XM_005267019.3:c.519+71_519+72insAC	XP_005267076.1:n.519+71_519+72insAC
XM_006715502.1:c.340-3086_340-3085insAC	XP_006715565.1:n.340-3086_340-3085insAC
XM_011535900.1:c.526+20623_526+20624insAC	XP_011534202.1:n.526+20623_526+20624insAC
XM_005267019.4:c.519+71_519+72insAC	XP_005267076.1:n.519+71_519+72insAC
XM_006715502.2:c.340-3086_340-3085insAC	XP_006715565.1:n.340-3086_340-3085insAC
XM_017010934.2:c.526+20623_526+20624insAC	XP_016866423.1:n.526+20623_526+20624insAC
NM_000288.4:c.633+71_633+72insAC MANE Select	NP_000279.1:n.633+71_633+72insAC