Canonical Allele Identifier: CA3134712012

Gene: PEX7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136866718G= , CM000668.2:g.136866718G=	GRCh38
NC_000006.11:g.137187856G= , CM000668.1:g.137187856G=	GRCh37
NC_000006.10:g.137229549G=	NCBI36
NG_008462.1:g.49139G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318471.5:c.618G= MANE Select	ENSP00000315680.3:p.Trp206=
ENST00000541292.6:c.618G=	ENSP00000441004.1:p.Trp206=
ENST00000678002.1:c.306G=
ENST00000678557.1:c.504G=	ENSP00000502962.1:p.Trp168=
ENST00000678593.1:c.623G=	ENSP00000503841.1:n.623G=
ENST00000679286.1:c.498G=	ENSP00000503168.1:p.Trp166=
ENST00000318471.4:c.618G=	ENSP00000315680.3:p.Trp206=
ENST00000541292.5:c.618G=	ENSP00000441004.1:p.Trp206=
NM_000288.3:c.618G=	NP_000279.1:p.Trp206=
XM_005267019.3:c.504G=	XP_005267076.1:p.Trp168=
XM_006715502.1:c.340-3172G=	XP_006715565.1:n.340-3172G=
XM_011535900.1:c.526+20537G=	XP_011534202.1:n.526+20537G=
XM_005267019.4:c.504G=	XP_005267076.1:p.Trp168=
XM_006715502.2:c.340-3172G=	XP_006715565.1:n.340-3172G=
XM_017010934.2:c.526+20537G=	XP_016866423.1:n.526+20537G=
NM_000288.4:c.618G= MANE Select	NP_000279.1:p.Trp206=