Canonical Allele Identifier: CA1729158015

Gene: CYP3A5 ZSCAN25

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99648351A= , CM000669.2:g.99648351A=	GRCh38
NC_000007.13:g.99245974A= , CM000669.1:g.99245974A=	GRCh37
NC_000007.12:g.99083910A=	NCBI36
NG_007938.1:g.36648T=
NG_007938.2:g.36648T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000646887.1:c.*1148T= (CYP3A5)	ENSP00000496704.1:n.*1148T=
ENST00000222982.8:c.1463T= (CYP3A5) MANE Select	ENSP00000222982.4:p.Ile488=
ENST00000339843.6:c.*2947T= (CYP3A5)	ENSP00000343074.2:n.*2947T=
ENST00000461920.5:n.2055T= (CYP3A5)
ENST00000469887.5:n.2996T= (CYP3A5)
NM_000777.4:c.1463T= (CYP3A5)	NP_000768.1:p.Ile488=
NM_001291829.1:c.1124T= (CYP3A5)	NP_001278758.1:p.Ile375=
NM_001291830.1:c.1433T= (CYP3A5)	NP_001278759.1:p.Ile478=
NR_033807.2:n.3197T= (CYP3A5)
XM_011515843.1:c.1124T= (CYP3A5)	XP_011514145.1:p.Ile375=
XM_011515844.1:c.1124T= (CYP3A5)	XP_011514146.1:p.Ile375=
XM_011515845.1:c.923T= (CYP3A5)	XP_011514147.1:p.Ile308=
XM_011515846.1:c.923T= (CYP3A5)	XP_011514148.1:p.Ile308=
XM_011515847.1:c.923T= (CYP3A5)	XP_011514149.1:p.Ile308=
XM_011515909.1:c.806-20744A= (ZSCAN25)	XP_011514211.1:n.806-20744A=
XR_927402.1:n.1466+24171A= (ZSCAN25)
NM_000777.5:c.1463T= (CYP3A5) MANE Select	NP_000768.1:p.Ile488=
NM_001350984.1:c.806-20744A= (ZSCAN25)	NP_001337913.1:n.806-20744A=
NM_001350985.1:c.806-20744A= (ZSCAN25)	NP_001337914.1:n.806-20744A=
XM_011515909.2:c.806-20744A= (ZSCAN25)	XP_011514211.1:n.806-20744A=
XR_927402.2:n.1465+24171A= (ZSCAN25)
NM_001291829.2:c.1124T= (CYP3A5)	NP_001278758.1:p.Ile375=
NM_001291830.2:c.1433T= (CYP3A5)	NP_001278759.1:p.Ile478=
NM_001350984.2:c.806-20744A= (ZSCAN25)	NP_001337913.1:n.806-20744A=
NM_001350985.2:c.806-20744A= (ZSCAN25)	NP_001337914.1:n.806-20744A=
NR_033807.3:n.3167T= (CYP3A5)