Canonical Allele Identifier: CA2680489792

Gene: PEX7

Linked Data

• gnomAD v4: 6-136866605-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136866605A>T , CM000668.2:g.136866605A>T	GRCh38
NC_000006.11:g.137187743A>T , CM000668.1:g.137187743A>T	GRCh37
NC_000006.10:g.137229436A>T	NCBI36
NG_008462.1:g.49026A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.527-22A>T MANE Select	ENSP00000315680.3:n.527-22A>T
ENST00000541292.6:c.527-22A>T	ENSP00000441004.1:n.527-22A>T
ENST00000678002.1:c.215-22A>T
ENST00000678557.1:c.413-22A>T	ENSP00000502962.1:n.413-22A>T
ENST00000678593.1:c.532-22A>T	ENSP00000503841.1:n.532-22A>T
ENST00000679286.1:c.407-22A>T	ENSP00000503168.1:n.407-22A>T
ENST00000318471.4:c.527-22A>T	ENSP00000315680.3:n.527-22A>T
ENST00000541292.5:c.527-22A>T	ENSP00000441004.1:n.527-22A>T
NM_000288.3:c.527-22A>T	NP_000279.1:n.527-22A>T
XM_005267019.3:c.413-22A>T	XP_005267076.1:n.413-22A>T
XM_006715502.1:c.340-3285A>T	XP_006715565.1:n.340-3285A>T
XM_011535900.1:c.526+20424A>T	XP_011534202.1:n.526+20424A>T
XM_005267019.4:c.413-22A>T	XP_005267076.1:n.413-22A>T
XM_006715502.2:c.340-3285A>T	XP_006715565.1:n.340-3285A>T
XM_017010934.2:c.526+20424A>T	XP_016866423.1:n.526+20424A>T
NM_000288.4:c.527-22A>T MANE Select	NP_000279.1:n.527-22A>T