Canonical Allele Identifier: CA1729185544

Gene: CYP3A5 ZSCAN25

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99676194G= , CM000669.2:g.99676194G=	GRCh38
NC_000007.13:g.99273817G= , CM000669.1:g.99273817G=	GRCh37
NC_000007.12:g.99111753G=	NCBI36
NG_007938.1:g.8805C=
NG_007938.2:g.8805C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439761.3:c.86C= (CYP3A5)	ENSP00000401269.1:p.Thr29=
ENST00000646887.1:c.86C= (CYP3A5)	ENSP00000496704.1:p.Thr29=
ENST00000222982.8:c.86C= (CYP3A5) MANE Select	ENSP00000222982.4:p.Thr29=
ENST00000339843.6:c.*334C= (CYP3A5)	ENSP00000343074.2:n.*334C=
ENST00000439761.1:c.86C= (CYP3A5)	ENSP00000401269.1:p.Thr29=
ENST00000456417.5:c.*226C= (CYP3A5)	ENSP00000415399.1:n.*226C=
ENST00000461920.5:n.546C= (CYP3A5)
ENST00000463364.5:n.156C= (CYP3A5)
ENST00000463907.5:n.186C= (CYP3A5)
ENST00000466061.5:n.186C= (CYP3A5)
ENST00000469622.5:n.183C= (CYP3A5)
ENST00000469887.5:n.383C= (CYP3A5)
ENST00000480723.5:n.143C= (CYP3A5)
ENST00000481825.5:n.554C= (CYP3A5)
ENST00000489231.1:n.183C= (CYP3A5)
NM_000777.4:c.86C= (CYP3A5)	NP_000768.1:p.Thr29=
NM_001190484.2:c.86C= (CYP3A5)	NP_001177413.1:p.Thr29=
NM_001291829.1:c.-386C= (CYP3A5)	NP_001278758.1:n.-386C=
NM_001291830.1:c.56C= (CYP3A5)	NP_001278759.1:p.Thr19=
NR_033807.2:n.584C= (CYP3A5)
XM_006715859.2:c.86C= (CYP3A5)	XP_006715922.1:p.Thr29=
XM_011515843.1:c.-404C= (CYP3A5)	XP_011514145.1:n.-404C=
XM_011515844.1:c.-362C= (CYP3A5)	XP_011514146.1:n.-362C=
XM_011515845.1:c.-596C= (CYP3A5)	XP_011514147.1:n.-596C=
XM_011515846.1:c.-464C= (CYP3A5)	XP_011514148.1:n.-464C=
XM_011515847.1:c.-704C= (CYP3A5)	XP_011514149.1:n.-704C=
XR_927383.1:n.211C= (CYP3A5)
XR_927402.1:n.1467-47281G= (ZSCAN25)
NM_000777.5:c.86C= (CYP3A5) MANE Select	NP_000768.1:p.Thr29=
XR_927402.2:n.1466-47281G= (ZSCAN25)
NM_001190484.3:c.86C= (CYP3A5)	NP_001177413.1:p.Thr29=
NM_001291829.2:c.-386C= (CYP3A5)	NP_001278758.1:n.-386C=
NM_001291830.2:c.56C= (CYP3A5)	NP_001278759.1:p.Thr19=
NR_033807.3:n.554C= (CYP3A5)