Canonical Allele Identifier: CA3135552379

Gene: PEX7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136866625A= , CM000668.2:g.136866625A=	GRCh38
NC_000006.11:g.137187763A= , CM000668.1:g.137187763A=	GRCh37
NC_000006.10:g.137229456A=	NCBI36
NG_008462.1:g.49046A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.527-2A= MANE Select	ENSP00000315680.3:n.527-2A=
ENST00000541292.6:c.527-2A=	ENSP00000441004.1:n.527-2A=
ENST00000678002.1:c.215-2A=
ENST00000678557.1:c.413-2A=	ENSP00000502962.1:n.413-2A=
ENST00000678593.1:c.532-2A=	ENSP00000503841.1:n.532-2A=
ENST00000679286.1:c.407-2A=	ENSP00000503168.1:n.407-2A=
ENST00000318471.4:c.527-2A=	ENSP00000315680.3:n.527-2A=
ENST00000541292.5:c.527-2A=	ENSP00000441004.1:n.527-2A=
NM_000288.3:c.527-2A=	NP_000279.1:n.527-2A=
XM_005267019.3:c.413-2A=	XP_005267076.1:n.413-2A=
XM_006715502.1:c.340-3265A=	XP_006715565.1:n.340-3265A=
XM_011535900.1:c.526+20444A=	XP_011534202.1:n.526+20444A=
XM_005267019.4:c.413-2A=	XP_005267076.1:n.413-2A=
XM_006715502.2:c.340-3265A=	XP_006715565.1:n.340-3265A=
XM_017010934.2:c.526+20444A=	XP_016866423.1:n.526+20444A=
NM_000288.4:c.527-2A= MANE Select	NP_000279.1:n.527-2A=