Canonical Allele Identifier: CA2680489825

Gene: PEX7

Linked Data

• gnomAD v4: 6-136866759-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136866759C>A , CM000668.2:g.136866759C>A	GRCh38
NC_000006.11:g.137187897C>A , CM000668.1:g.137187897C>A	GRCh37
NC_000006.10:g.137229590C>A	NCBI36
NG_008462.1:g.49180C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.633+26C>A MANE Select	ENSP00000315680.3:n.633+26C>A
ENST00000541292.6:c.633+26C>A	ENSP00000441004.1:n.633+26C>A
ENST00000678002.1:c.321+26C>A
ENST00000678557.1:c.519+26C>A	ENSP00000502962.1:n.519+26C>A
ENST00000678593.1:c.638+26C>A	ENSP00000503841.1:n.638+26C>A
ENST00000679286.1:c.513+26C>A	ENSP00000503168.1:n.513+26C>A
ENST00000318471.4:c.633+26C>A	ENSP00000315680.3:n.633+26C>A
ENST00000541292.5:c.633+26C>A	ENSP00000441004.1:n.633+26C>A
NM_000288.3:c.633+26C>A	NP_000279.1:n.633+26C>A
XM_005267019.3:c.519+26C>A	XP_005267076.1:n.519+26C>A
XM_006715502.1:c.340-3131C>A	XP_006715565.1:n.340-3131C>A
XM_011535900.1:c.526+20578C>A	XP_011534202.1:n.526+20578C>A
XM_005267019.4:c.519+26C>A	XP_005267076.1:n.519+26C>A
XM_006715502.2:c.340-3131C>A	XP_006715565.1:n.340-3131C>A
XM_017010934.2:c.526+20578C>A	XP_016866423.1:n.526+20578C>A
NM_000288.4:c.633+26C>A MANE Select	NP_000279.1:n.633+26C>A