Canonical Allele Identifier: CA3135028871

Gene: PEX7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136826407C= , CM000668.2:g.136826407C=	GRCh38
NC_000006.11:g.137147545C= , CM000668.1:g.137147545C=	GRCh37
NC_000006.10:g.137189238C=	NCBI36
NG_008462.1:g.8828C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.277C= MANE Select	ENSP00000315680.3:p.Gln93=
ENST00000541292.6:c.277C=	ENSP00000441004.1:p.Gln93=
ENST00000678002.1:c.152C=
ENST00000678557.1:c.163C=	ENSP00000502962.1:p.Gln55=
ENST00000678593.1:c.282C=	ENSP00000503841.1:n.282C=
ENST00000679286.1:c.157C=	ENSP00000503168.1:p.Gln53=
ENST00000318471.4:c.277C=	ENSP00000315680.3:p.Gln93=
ENST00000367756.8:c.277C=	ENSP00000356730.4:p.Gln93=
ENST00000541292.5:c.277C=	ENSP00000441004.1:p.Gln93=
NM_000288.3:c.277C=	NP_000279.1:p.Gln93=
XM_005267019.3:c.163C=	XP_005267076.1:p.Gln55=
XM_006715502.1:c.277C=	XP_006715565.1:p.Gln93=
XM_011535900.1:c.277C=	XP_011534202.1:p.Gln93=
XM_005267019.4:c.163C=	XP_005267076.1:p.Gln55=
XM_006715502.2:c.277C=	XP_006715565.1:p.Gln93=
XM_017010934.2:c.277C=	XP_016866423.1:p.Gln93=
NM_000288.4:c.277C= MANE Select	NP_000279.1:p.Gln93=