Canonical Allele Identifier: CA1729157879

Gene: CYP3A5 ZSCAN25

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99648254G= , CM000669.2:g.99648254G=	GRCh38
NC_000007.13:g.99245877G= , CM000669.1:g.99245877G=	GRCh37
NC_000007.12:g.99083813G=	NCBI36
NG_007938.1:g.36745C=
NG_007938.2:g.36745C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646887.1:c.*1245C= (CYP3A5)	ENSP00000496704.1:n.*1245C=
ENST00000222982.8:c.*51C= (CYP3A5) MANE Select	ENSP00000222982.4:n.*51C=
ENST00000339843.6:c.*3044C= (CYP3A5)	ENSP00000343074.2:n.*3044C=
ENST00000461920.5:n.2152C= (CYP3A5)
ENST00000469887.5:n.3093C= (CYP3A5)
NM_000777.4:c.*51C= (CYP3A5)	NP_000768.1:n.*51C=
NM_001291829.1:c.*51C= (CYP3A5)	NP_001278758.1:n.*51C=
NM_001291830.1:c.*51C= (CYP3A5)	NP_001278759.1:n.*51C=
NR_033807.2:n.3294C= (CYP3A5)
XM_011515843.1:c.*51C= (CYP3A5)	XP_011514145.1:n.*51C=
XM_011515844.1:c.*51C= (CYP3A5)	XP_011514146.1:n.*51C=
XM_011515845.1:c.*51C= (CYP3A5)	XP_011514147.1:n.*51C=
XM_011515846.1:c.*51C= (CYP3A5)	XP_011514148.1:n.*51C=
XM_011515847.1:c.*51C= (CYP3A5)	XP_011514149.1:n.*51C=
XM_011515909.1:c.806-20841G= (ZSCAN25)	XP_011514211.1:n.806-20841G=
XM_011515910.1:c.*731G= (ZSCAN25)	XP_011514212.1:n.*731G=
XR_927402.1:n.1466+24074G= (ZSCAN25)
NM_000777.5:c.*51C= (CYP3A5) MANE Select	NP_000768.1:n.*51C=
NM_001350984.1:c.806-20841G= (ZSCAN25)	NP_001337913.1:n.806-20841G=
NM_001350985.1:c.806-20841G= (ZSCAN25)	NP_001337914.1:n.806-20841G=
XM_011515909.2:c.806-20841G= (ZSCAN25)	XP_011514211.1:n.806-20841G=
XR_927402.2:n.1465+24074G= (ZSCAN25)
NM_001291829.2:c.*51C= (CYP3A5)	NP_001278758.1:n.*51C=
NM_001291830.2:c.*51C= (CYP3A5)	NP_001278759.1:n.*51C=
NM_001350984.2:c.806-20841G= (ZSCAN25)	NP_001337913.1:n.806-20841G=
NM_001350985.2:c.806-20841G= (ZSCAN25)	NP_001337914.1:n.806-20841G=
NR_033807.3:n.3264C= (CYP3A5)