Canonical Allele Identifier: CA1729185521

Gene: CYP3A5 ZSCAN25

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99676181A= , CM000669.2:g.99676181A=	GRCh38
NC_000007.13:g.99273804A= , CM000669.1:g.99273804A=	GRCh37
NC_000007.12:g.99111740A=	NCBI36
NG_007938.1:g.8818T=
NG_007938.2:g.8818T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439761.3:c.99T= (CYP3A5)	ENSP00000401269.1:p.Phe33=
ENST00000646887.1:c.99T= (CYP3A5)	ENSP00000496704.1:p.Phe33=
ENST00000222982.8:c.99T= (CYP3A5) MANE Select	ENSP00000222982.4:p.Phe33=
ENST00000339843.6:c.*347T= (CYP3A5)	ENSP00000343074.2:n.*347T=
ENST00000439761.1:c.99T= (CYP3A5)	ENSP00000401269.1:p.Phe33=
ENST00000456417.5:c.*239T= (CYP3A5)	ENSP00000415399.1:n.*239T=
ENST00000461920.5:n.559T= (CYP3A5)
ENST00000463364.5:n.169T= (CYP3A5)
ENST00000463907.5:n.199T= (CYP3A5)
ENST00000466061.5:n.199T= (CYP3A5)
ENST00000469622.5:n.196T= (CYP3A5)
ENST00000469887.5:n.396T= (CYP3A5)
ENST00000480723.5:n.156T= (CYP3A5)
ENST00000481825.5:n.567T= (CYP3A5)
ENST00000489231.1:n.196T= (CYP3A5)
NM_000777.4:c.99T= (CYP3A5)	NP_000768.1:p.Phe33=
NM_001190484.2:c.99T= (CYP3A5)	NP_001177413.1:p.Phe33=
NM_001291829.1:c.-373T= (CYP3A5)	NP_001278758.1:n.-373T=
NM_001291830.1:c.69T= (CYP3A5)	NP_001278759.1:p.Phe23=
NR_033807.2:n.597T= (CYP3A5)
XM_006715859.2:c.99T= (CYP3A5)	XP_006715922.1:p.Phe33=
XM_011515843.1:c.-391T= (CYP3A5)	XP_011514145.1:n.-391T=
XM_011515844.1:c.-349T= (CYP3A5)	XP_011514146.1:n.-349T=
XM_011515845.1:c.-583T= (CYP3A5)	XP_011514147.1:n.-583T=
XM_011515846.1:c.-451T= (CYP3A5)	XP_011514148.1:n.-451T=
XM_011515847.1:c.-691T= (CYP3A5)	XP_011514149.1:n.-691T=
XR_927383.1:n.224T= (CYP3A5)
XR_927402.1:n.1467-47294A= (ZSCAN25)
NM_000777.5:c.99T= (CYP3A5) MANE Select	NP_000768.1:p.Phe33=
XR_927402.2:n.1466-47294A= (ZSCAN25)
NM_001190484.3:c.99T= (CYP3A5)	NP_001177413.1:p.Phe33=
NM_001291829.2:c.-373T= (CYP3A5)	NP_001278758.1:n.-373T=
NM_001291830.2:c.69T= (CYP3A5)	NP_001278759.1:p.Phe23=
NR_033807.3:n.567T= (CYP3A5)