Canonical Allele Identifier: CA3134712005

Gene: PEX7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136822705A= , CM000668.2:g.136822705A=	GRCh38
NC_000006.11:g.137143843A= , CM000668.1:g.137143843A=	GRCh37
NC_000006.10:g.137185536A=	NCBI36
NG_008462.1:g.5126A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.40A= MANE Select	ENSP00000315680.3:p.Thr14=
ENST00000541292.6:c.40A=	ENSP00000441004.1:p.Thr14=
ENST00000678593.1:c.40A=	ENSP00000503841.1:p.Thr14=
ENST00000318471.4:c.40A=	ENSP00000315680.3:p.Thr14=
ENST00000367756.8:c.40A=	ENSP00000356730.4:p.Thr14=
ENST00000541292.5:c.40A=	ENSP00000441004.1:p.Thr14=
NM_000288.3:c.40A=	NP_000279.1:p.Thr14=
XM_006715502.1:c.40A=	XP_006715565.1:p.Thr14=
XM_011535900.1:c.40A=	XP_011534202.1:p.Thr14=
XM_006715502.2:c.40A=	XP_006715565.1:p.Thr14=
XM_017010934.2:c.40A=	XP_016866423.1:p.Thr14=
NM_000288.4:c.40A= MANE Select	NP_000279.1:p.Thr14=