Canonical Allele Identifier: CA2832584248

Gene: PEX7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136822621C= , CM000668.2:g.136822621C=	GRCh38
NC_000006.11:g.137143759C= , CM000668.1:g.137143759C=	GRCh37
NC_000006.10:g.137185452C=	NCBI36
NG_008462.1:g.5042C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.-45C= MANE Select	ENSP00000315680.3:n.-45C=
ENST00000541292.6:c.-45C=	ENSP00000441004.1:n.-45C=
ENST00000318471.4:c.-45C=	ENSP00000315680.3:n.-45C=
ENST00000367756.8:c.-45C=	ENSP00000356730.4:n.-45C=
ENST00000541292.5:c.-45C=	ENSP00000441004.1:n.-45C=
NM_000288.3:c.-45C=	NP_000279.1:n.-45C=
XM_006715502.1:c.-45C=	XP_006715565.1:n.-45C=
XM_011535900.1:c.-45C=	XP_011534202.1:n.-45C=
XM_006715502.2:c.-45C=	XP_006715565.1:n.-45C=
XM_017010934.2:c.-45C=	XP_016866423.1:n.-45C=
NM_000288.4:c.-45C= MANE Select	NP_000279.1:n.-45C=