Canonical Allele Identifier: CA2680489115

Gene: PEX7

Linked Data

• gnomAD v4: 6-136826247-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136826249dup , CM000668.2:g.136826249dup	GRCh38
NC_000006.11:g.137147387dup , CM000668.1:g.137147387dup	GRCh37
NC_000006.10:g.137189080dup	NCBI36
NG_008462.1:g.8670dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.189-70dup MANE Select	ENSP00000315680.3:n.189-70dup
ENST00000541292.6:c.189-70dup	ENSP00000441004.1:n.189-70dup
ENST00000678002.1:c.59-65dup
ENST00000678557.1:c.75-70dup	ENSP00000502962.1:n.75-70dup
ENST00000678593.1:c.189-65dup	ENSP00000503841.1:n.189-65dup
ENST00000679286.1:c.69-70dup	ENSP00000503168.1:n.69-70dup
ENST00000318471.4:c.189-70dup	ENSP00000315680.3:n.189-70dup
ENST00000367756.8:c.189-70dup	ENSP00000356730.4:n.189-70dup
ENST00000541292.5:c.189-70dup	ENSP00000441004.1:n.189-70dup
NM_000288.3:c.189-70dup	NP_000279.1:n.189-70dup
XM_005267019.3:c.75-70dup	XP_005267076.1:n.75-70dup
XM_006715502.1:c.189-70dup	XP_006715565.1:n.189-70dup
XM_011535900.1:c.189-70dup	XP_011534202.1:n.189-70dup
XM_005267019.4:c.75-70dup	XP_005267076.1:n.75-70dup
XM_006715502.2:c.189-70dup	XP_006715565.1:n.189-70dup
XM_017010934.2:c.189-70dup	XP_016866423.1:n.189-70dup
NM_000288.4:c.189-70dup MANE Select	NP_000279.1:n.189-70dup