Canonical Allele Identifier: CA1729173603

Gene: CYP3A5 ZSCAN25

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99665199A= , CM000669.2:g.99665199A=	GRCh38
NC_000007.13:g.99262822A= , CM000669.1:g.99262822A=	GRCh37
NC_000007.12:g.99100758A=	NCBI36
NG_007938.1:g.19800T=
NG_007938.2:g.19800T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646887.1:c.*322T= (CYP3A5)	ENSP00000496704.1:n.*322T=
ENST00000222982.8:c.637T= (CYP3A5) MANE Select	ENSP00000222982.4:p.Phe213=
ENST00000339843.6:c.*1036T= (CYP3A5)	ENSP00000343074.2:n.*1036T=
ENST00000461920.5:n.1229T= (CYP3A5)
ENST00000463364.5:n.956T= (CYP3A5)
ENST00000466061.5:n.977T= (CYP3A5)
ENST00000469887.5:n.1085T= (CYP3A5)
ENST00000481825.5:n.1237T= (CYP3A5)
NM_000777.4:c.637T= (CYP3A5)	NP_000768.1:p.Phe213=
NM_001291829.1:c.298T= (CYP3A5)	NP_001278758.1:p.Phe100=
NM_001291830.1:c.607T= (CYP3A5)	NP_001278759.1:p.Phe203=
NR_033807.2:n.1286T= (CYP3A5)
XM_006715859.2:c.637T= (CYP3A5)	XP_006715922.1:p.Phe213=
XM_011515843.1:c.298T= (CYP3A5)	XP_011514145.1:p.Phe100=
XM_011515844.1:c.298T= (CYP3A5)	XP_011514146.1:p.Phe100=
XM_011515845.1:c.97T= (CYP3A5)	XP_011514147.1:p.Phe33=
XM_011515846.1:c.97T= (CYP3A5)	XP_011514148.1:p.Phe33=
XM_011515847.1:c.97T= (CYP3A5)	XP_011514149.1:p.Phe33=
XM_011515909.1:c.806-3896A= (ZSCAN25)	XP_011514211.1:n.806-3896A=
XR_927402.1:n.1466+41019A= (ZSCAN25)
NM_000777.5:c.637T= (CYP3A5) MANE Select	NP_000768.1:p.Phe213=
NM_001350984.1:c.806-3896A= (ZSCAN25)	NP_001337913.1:n.806-3896A=
NM_001350985.1:c.806-3896A= (ZSCAN25)	NP_001337914.1:n.806-3896A=
XM_011515909.2:c.806-3896A= (ZSCAN25)	XP_011514211.1:n.806-3896A=
XR_927402.2:n.1465+41019A= (ZSCAN25)
NM_001291829.2:c.298T= (CYP3A5)	NP_001278758.1:p.Phe100=
NM_001291830.2:c.607T= (CYP3A5)	NP_001278759.1:p.Phe203=
NM_001350984.2:c.806-3896A= (ZSCAN25)	NP_001337913.1:n.806-3896A=
NM_001350985.2:c.806-3896A= (ZSCAN25)	NP_001337914.1:n.806-3896A=
NR_033807.3:n.1256T= (CYP3A5)