Canonical Allele Identifier: CA1729185446

Gene: CYP3A5 ZSCAN25

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99676133A= , CM000669.2:g.99676133A=	GRCh38
NC_000007.13:g.99273756A= , CM000669.1:g.99273756A=	GRCh37
NC_000007.12:g.99111692A=	NCBI36
NG_007938.1:g.8866T=
NG_007938.2:g.8866T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439761.3:c.147T= (CYP3A5)	ENSP00000401269.1:p.Asn49=
ENST00000646887.1:c.147T= (CYP3A5)	ENSP00000496704.1:p.Asn49=
ENST00000222982.8:c.147T= (CYP3A5) MANE Select	ENSP00000222982.4:p.Asn49=
ENST00000339843.6:c.*395T= (CYP3A5)	ENSP00000343074.2:n.*395T=
ENST00000439761.1:c.147T= (CYP3A5)	ENSP00000401269.1:p.Asn49=
ENST00000456417.5:c.*287T= (CYP3A5)	ENSP00000415399.1:n.*287T=
ENST00000461920.5:n.607T= (CYP3A5)
ENST00000463364.5:n.217T= (CYP3A5)
ENST00000463907.5:n.247T= (CYP3A5)
ENST00000466061.5:n.247T= (CYP3A5)
ENST00000469622.5:n.244T= (CYP3A5)
ENST00000469887.5:n.444T= (CYP3A5)
ENST00000480723.5:n.204T= (CYP3A5)
ENST00000481825.5:n.615T= (CYP3A5)
ENST00000489231.1:n.244T= (CYP3A5)
NM_000777.4:c.147T= (CYP3A5)	NP_000768.1:p.Asn49=
NM_001190484.2:c.147T= (CYP3A5)	NP_001177413.1:p.Asn49=
NM_001291829.1:c.-325T= (CYP3A5)	NP_001278758.1:n.-325T=
NM_001291830.1:c.117T= (CYP3A5)	NP_001278759.1:p.Asn39=
NR_033807.2:n.645T= (CYP3A5)
XM_006715859.2:c.147T= (CYP3A5)	XP_006715922.1:p.Asn49=
XM_011515843.1:c.-343T= (CYP3A5)	XP_011514145.1:n.-343T=
XM_011515844.1:c.-301T= (CYP3A5)	XP_011514146.1:n.-301T=
XM_011515845.1:c.-535T= (CYP3A5)	XP_011514147.1:n.-535T=
XM_011515846.1:c.-403T= (CYP3A5)	XP_011514148.1:n.-403T=
XM_011515847.1:c.-643T= (CYP3A5)	XP_011514149.1:n.-643T=
XR_927383.1:n.272T= (CYP3A5)
XR_927402.1:n.1467-47342A= (ZSCAN25)
NM_000777.5:c.147T= (CYP3A5) MANE Select	NP_000768.1:p.Asn49=
XR_927402.2:n.1466-47342A= (ZSCAN25)
NM_001190484.3:c.147T= (CYP3A5)	NP_001177413.1:p.Asn49=
NM_001291829.2:c.-325T= (CYP3A5)	NP_001278758.1:n.-325T=
NM_001291830.2:c.117T= (CYP3A5)	NP_001278759.1:p.Asn39=
NR_033807.3:n.615T= (CYP3A5)