Canonical Allele Identifier: CA3134742741

Gene: PEX7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136869905G= , CM000668.2:g.136869905G=	GRCh38
NC_000006.11:g.137191043G= , CM000668.1:g.137191043G=	GRCh37
NC_000006.10:g.137232736G=	NCBI36
NG_008462.1:g.52326G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.649G= MANE Select	ENSP00000315680.3:p.Gly217=
ENST00000541292.6:c.649G=	ENSP00000441004.1:p.Gly217=
ENST00000678002.1:c.337G=
ENST00000678557.1:c.535G=	ENSP00000502962.1:p.Gly179=
ENST00000678593.1:c.654G=	ENSP00000503841.1:n.654G=
ENST00000679286.1:c.529G=	ENSP00000503168.1:p.Gly177=
ENST00000318471.4:c.649G=	ENSP00000315680.3:p.Gly217=
ENST00000541292.5:c.649G=	ENSP00000441004.1:p.Gly217=
NM_000288.3:c.649G=	NP_000279.1:p.Gly217=
XM_005267019.3:c.535G=	XP_005267076.1:p.Gly179=
XM_006715502.1:c.355G=	XP_006715565.1:p.Gly119=
XM_011535900.1:c.526+23724G=	XP_011534202.1:n.526+23724G=
XM_005267019.4:c.535G=	XP_005267076.1:p.Gly179=
XM_006715502.2:c.355G=	XP_006715565.1:p.Gly119=
XM_017010934.2:c.526+23724G=	XP_016866423.1:n.526+23724G=
NM_000288.4:c.649G= MANE Select	NP_000279.1:p.Gly217=