Canonical Allele Identifier: CA1729185539

Gene: CYP3A5 ZSCAN25

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99676192G= , CM000669.2:g.99676192G=	GRCh38
NC_000007.13:g.99273815G= , CM000669.1:g.99273815G=	GRCh37
NC_000007.12:g.99111751G=	NCBI36
NG_007938.1:g.8807C=
NG_007938.2:g.8807C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439761.3:c.88C= (CYP3A5)	ENSP00000401269.1:p.His30=
ENST00000646887.1:c.88C= (CYP3A5)	ENSP00000496704.1:p.His30=
ENST00000222982.8:c.88C= (CYP3A5) MANE Select	ENSP00000222982.4:p.His30=
ENST00000339843.6:c.*336C= (CYP3A5)	ENSP00000343074.2:n.*336C=
ENST00000439761.1:c.88C= (CYP3A5)	ENSP00000401269.1:p.His30=
ENST00000456417.5:c.*228C= (CYP3A5)	ENSP00000415399.1:n.*228C=
ENST00000461920.5:n.548C= (CYP3A5)
ENST00000463364.5:n.158C= (CYP3A5)
ENST00000463907.5:n.188C= (CYP3A5)
ENST00000466061.5:n.188C= (CYP3A5)
ENST00000469622.5:n.185C= (CYP3A5)
ENST00000469887.5:n.385C= (CYP3A5)
ENST00000480723.5:n.145C= (CYP3A5)
ENST00000481825.5:n.556C= (CYP3A5)
ENST00000489231.1:n.185C= (CYP3A5)
NM_000777.4:c.88C= (CYP3A5)	NP_000768.1:p.His30=
NM_001190484.2:c.88C= (CYP3A5)	NP_001177413.1:p.His30=
NM_001291829.1:c.-384C= (CYP3A5)	NP_001278758.1:n.-384C=
NM_001291830.1:c.58C= (CYP3A5)	NP_001278759.1:p.His20=
NR_033807.2:n.586C= (CYP3A5)
XM_006715859.2:c.88C= (CYP3A5)	XP_006715922.1:p.His30=
XM_011515843.1:c.-402C= (CYP3A5)	XP_011514145.1:n.-402C=
XM_011515844.1:c.-360C= (CYP3A5)	XP_011514146.1:n.-360C=
XM_011515845.1:c.-594C= (CYP3A5)	XP_011514147.1:n.-594C=
XM_011515846.1:c.-462C= (CYP3A5)	XP_011514148.1:n.-462C=
XM_011515847.1:c.-702C= (CYP3A5)	XP_011514149.1:n.-702C=
XR_927383.1:n.213C= (CYP3A5)
XR_927402.1:n.1467-47283G= (ZSCAN25)
NM_000777.5:c.88C= (CYP3A5) MANE Select	NP_000768.1:p.His30=
XR_927402.2:n.1466-47283G= (ZSCAN25)
NM_001190484.3:c.88C= (CYP3A5)	NP_001177413.1:p.His30=
NM_001291829.2:c.-384C= (CYP3A5)	NP_001278758.1:n.-384C=
NM_001291830.2:c.58C= (CYP3A5)	NP_001278759.1:p.His20=
NR_033807.3:n.556C= (CYP3A5)