Canonical Allele Identifier: CA1729185550

Gene: CYP3A5 ZSCAN25

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99676197C= , CM000669.2:g.99676197C=	GRCh38
NC_000007.13:g.99273820C= , CM000669.1:g.99273820C=	GRCh37
NC_000007.12:g.99111756C=	NCBI36
NG_007938.1:g.8802G=
NG_007938.2:g.8802G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439761.3:c.83G= (CYP3A5)	ENSP00000401269.1:p.Arg28=
ENST00000646887.1:c.83G= (CYP3A5)	ENSP00000496704.1:p.Arg28=
ENST00000222982.8:c.83G= (CYP3A5) MANE Select	ENSP00000222982.4:p.Arg28=
ENST00000339843.6:c.*331G= (CYP3A5)	ENSP00000343074.2:n.*331G=
ENST00000439761.1:c.83G= (CYP3A5)	ENSP00000401269.1:p.Arg28=
ENST00000456417.5:c.*223G= (CYP3A5)	ENSP00000415399.1:n.*223G=
ENST00000461920.5:n.543G= (CYP3A5)
ENST00000463364.5:n.153G= (CYP3A5)
ENST00000463907.5:n.183G= (CYP3A5)
ENST00000466061.5:n.183G= (CYP3A5)
ENST00000469622.5:n.180G= (CYP3A5)
ENST00000469887.5:n.380G= (CYP3A5)
ENST00000480723.5:n.140G= (CYP3A5)
ENST00000481825.5:n.551G= (CYP3A5)
ENST00000489231.1:n.180G= (CYP3A5)
NM_000777.4:c.83G= (CYP3A5)	NP_000768.1:p.Arg28=
NM_001190484.2:c.83G= (CYP3A5)	NP_001177413.1:p.Arg28=
NM_001291829.1:c.-389G= (CYP3A5)	NP_001278758.1:n.-389G=
NM_001291830.1:c.53G= (CYP3A5)	NP_001278759.1:p.Arg18=
NR_033807.2:n.581G= (CYP3A5)
XM_006715859.2:c.83G= (CYP3A5)	XP_006715922.1:p.Arg28=
XM_011515843.1:c.-407G= (CYP3A5)	XP_011514145.1:n.-407G=
XM_011515844.1:c.-365G= (CYP3A5)	XP_011514146.1:n.-365G=
XM_011515845.1:c.-599G= (CYP3A5)	XP_011514147.1:n.-599G=
XM_011515846.1:c.-467G= (CYP3A5)	XP_011514148.1:n.-467G=
XM_011515847.1:c.-707G= (CYP3A5)	XP_011514149.1:n.-707G=
XR_927383.1:n.208G= (CYP3A5)
XR_927402.1:n.1467-47278C= (ZSCAN25)
NM_000777.5:c.83G= (CYP3A5) MANE Select	NP_000768.1:p.Arg28=
XR_927402.2:n.1466-47278C= (ZSCAN25)
NM_001190484.3:c.83G= (CYP3A5)	NP_001177413.1:p.Arg28=
NM_001291829.2:c.-389G= (CYP3A5)	NP_001278758.1:n.-389G=
NM_001291830.2:c.53G= (CYP3A5)	NP_001278759.1:p.Arg18=
NR_033807.3:n.551G= (CYP3A5)