Canonical Allele Identifier: CA1729185563

Gene: CYP3A5 ZSCAN25

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99676200G= , CM000669.2:g.99676200G=	GRCh38
NC_000007.13:g.99273823G= , CM000669.1:g.99273823G=	GRCh37
NC_000007.12:g.99111759G=	NCBI36
NG_007938.1:g.8799C=
NG_007938.2:g.8799C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439761.3:c.80C= (CYP3A5)	ENSP00000401269.1:p.Thr27=
ENST00000646887.1:c.80C= (CYP3A5)	ENSP00000496704.1:p.Thr27=
ENST00000222982.8:c.80C= (CYP3A5) MANE Select	ENSP00000222982.4:p.Thr27=
ENST00000339843.6:c.*328C= (CYP3A5)	ENSP00000343074.2:n.*328C=
ENST00000439761.1:c.80C= (CYP3A5)	ENSP00000401269.1:p.Thr27=
ENST00000456417.5:c.*220C= (CYP3A5)	ENSP00000415399.1:n.*220C=
ENST00000461920.5:n.540C= (CYP3A5)
ENST00000463364.5:n.150C= (CYP3A5)
ENST00000463907.5:n.180C= (CYP3A5)
ENST00000466061.5:n.180C= (CYP3A5)
ENST00000469622.5:n.177C= (CYP3A5)
ENST00000469887.5:n.377C= (CYP3A5)
ENST00000480723.5:n.137C= (CYP3A5)
ENST00000481825.5:n.548C= (CYP3A5)
ENST00000489231.1:n.177C= (CYP3A5)
NM_000777.4:c.80C= (CYP3A5)	NP_000768.1:p.Thr27=
NM_001190484.2:c.80C= (CYP3A5)	NP_001177413.1:p.Thr27=
NM_001291829.1:c.-392C= (CYP3A5)	NP_001278758.1:n.-392C=
NM_001291830.1:c.50C= (CYP3A5)	NP_001278759.1:p.Thr17=
NR_033807.2:n.578C= (CYP3A5)
XM_006715859.2:c.80C= (CYP3A5)	XP_006715922.1:p.Thr27=
XM_011515843.1:c.-410C= (CYP3A5)	XP_011514145.1:n.-410C=
XM_011515844.1:c.-368C= (CYP3A5)	XP_011514146.1:n.-368C=
XM_011515845.1:c.-602C= (CYP3A5)	XP_011514147.1:n.-602C=
XM_011515846.1:c.-470C= (CYP3A5)	XP_011514148.1:n.-470C=
XM_011515847.1:c.-710C= (CYP3A5)	XP_011514149.1:n.-710C=
XR_927383.1:n.205C= (CYP3A5)
XR_927402.1:n.1467-47275G= (ZSCAN25)
NM_000777.5:c.80C= (CYP3A5) MANE Select	NP_000768.1:p.Thr27=
XR_927402.2:n.1466-47275G= (ZSCAN25)
NM_001190484.3:c.80C= (CYP3A5)	NP_001177413.1:p.Thr27=
NM_001291829.2:c.-392C= (CYP3A5)	NP_001278758.1:n.-392C=
NM_001291830.2:c.50C= (CYP3A5)	NP_001278759.1:p.Thr17=
NR_033807.3:n.548C= (CYP3A5)