Canonical Allele Identifier: CA1729173622

Gene: CYP3A5 ZSCAN25

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99665257G= , CM000669.2:g.99665257G=	GRCh38
NC_000007.13:g.99262880G= , CM000669.1:g.99262880G=	GRCh37
NC_000007.12:g.99100816G=	NCBI36
NG_007938.1:g.19742C=
NG_007938.2:g.19742C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646887.1:c.*264C= (CYP3A5)	ENSP00000496704.1:n.*264C=
ENST00000222982.8:c.579C= (CYP3A5) MANE Select	ENSP00000222982.4:p.Ile193=
ENST00000339843.6:c.*978C= (CYP3A5)	ENSP00000343074.2:n.*978C=
ENST00000461920.5:n.1171C= (CYP3A5)
ENST00000463364.5:n.898C= (CYP3A5)
ENST00000466061.5:n.919C= (CYP3A5)
ENST00000469887.5:n.1027C= (CYP3A5)
ENST00000481825.5:n.1179C= (CYP3A5)
NM_000777.4:c.579C= (CYP3A5)	NP_000768.1:p.Ile193=
NM_001291829.1:c.240C= (CYP3A5)	NP_001278758.1:p.Ile80=
NM_001291830.1:c.549C= (CYP3A5)	NP_001278759.1:p.Ile183=
NR_033807.2:n.1228C= (CYP3A5)
XM_006715859.2:c.579C= (CYP3A5)	XP_006715922.1:p.Ile193=
XM_011515843.1:c.240C= (CYP3A5)	XP_011514145.1:p.Ile80=
XM_011515844.1:c.240C= (CYP3A5)	XP_011514146.1:p.Ile80=
XM_011515845.1:c.39C= (CYP3A5)	XP_011514147.1:p.Ile13=
XM_011515846.1:c.39C= (CYP3A5)	XP_011514148.1:p.Ile13=
XM_011515847.1:c.39C= (CYP3A5)	XP_011514149.1:p.Ile13=
XM_011515909.1:c.806-3838G= (ZSCAN25)	XP_011514211.1:n.806-3838G=
XR_927402.1:n.1466+41077G= (ZSCAN25)
NM_000777.5:c.579C= (CYP3A5) MANE Select	NP_000768.1:p.Ile193=
NM_001350984.1:c.806-3838G= (ZSCAN25)	NP_001337913.1:n.806-3838G=
NM_001350985.1:c.806-3838G= (ZSCAN25)	NP_001337914.1:n.806-3838G=
XM_011515909.2:c.806-3838G= (ZSCAN25)	XP_011514211.1:n.806-3838G=
XR_927402.2:n.1465+41077G= (ZSCAN25)
NM_001291829.2:c.240C= (CYP3A5)	NP_001278758.1:p.Ile80=
NM_001291830.2:c.549C= (CYP3A5)	NP_001278759.1:p.Ile183=
NM_001350984.2:c.806-3838G= (ZSCAN25)	NP_001337913.1:n.806-3838G=
NM_001350985.2:c.806-3838G= (ZSCAN25)	NP_001337914.1:n.806-3838G=
NR_033807.3:n.1198C= (CYP3A5)