Canonical Allele Identifier: CA368361191

Gene: CYP3A5 ZSCAN25

Linked Data

• MyVariant Identifiers: chr7:g.99245983T>A (hg19) ; chr7:g.99648360T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99648360T>A , CM000669.2:g.99648360T>A	GRCh38
NC_000007.13:g.99245983T>A , CM000669.1:g.99245983T>A	GRCh37
NC_000007.12:g.99083919T>A	NCBI36
NG_007938.1:g.36639A>T
NG_007938.2:g.36639A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000646887.1:c.*1139A>T (CYP3A5)	ENSP00000496704.1:n.*1139A>T
ENST00000222982.8:c.1454A>T (CYP3A5) MANE Select	ENSP00000222982.4:p.Glu485Val
ENST00000339843.6:c.*2938A>T (CYP3A5)	ENSP00000343074.2:n.*2938A>T
ENST00000461920.5:n.2046A>T (CYP3A5)
ENST00000469887.5:n.2987A>T (CYP3A5)
NM_000777.4:c.1454A>T (CYP3A5)	NP_000768.1:p.Glu485Val
NM_001291829.1:c.1115A>T (CYP3A5)	NP_001278758.1:p.Glu372Val
NM_001291830.1:c.1424A>T (CYP3A5)	NP_001278759.1:p.Glu475Val
NR_033807.2:n.3188A>T (CYP3A5)
XM_011515843.1:c.1115A>T (CYP3A5)	XP_011514145.1:p.Glu372Val
XM_011515844.1:c.1115A>T (CYP3A5)	XP_011514146.1:p.Glu372Val
XM_011515845.1:c.914A>T (CYP3A5)	XP_011514147.1:p.Glu305Val
XM_011515846.1:c.914A>T (CYP3A5)	XP_011514148.1:p.Glu305Val
XM_011515847.1:c.914A>T (CYP3A5)	XP_011514149.1:p.Glu305Val
XM_011515909.1:c.806-20735T>A (ZSCAN25)	XP_011514211.1:n.806-20735T>A
XR_927402.1:n.1466+24180T>A (ZSCAN25)
NM_000777.5:c.1454A>T (CYP3A5) MANE Select	NP_000768.1:p.Glu485Val
NM_001350984.1:c.806-20735T>A (ZSCAN25)	NP_001337913.1:n.806-20735T>A
NM_001350985.1:c.806-20735T>A (ZSCAN25)	NP_001337914.1:n.806-20735T>A
XM_011515909.2:c.806-20735T>A (ZSCAN25)	XP_011514211.1:n.806-20735T>A
XR_927402.2:n.1465+24180T>A (ZSCAN25)
NM_001291829.2:c.1115A>T (CYP3A5)	NP_001278758.1:p.Glu372Val
NM_001291830.2:c.1424A>T (CYP3A5)	NP_001278759.1:p.Glu475Val
NM_001350984.2:c.806-20735T>A (ZSCAN25)	NP_001337913.1:n.806-20735T>A
NM_001350985.2:c.806-20735T>A (ZSCAN25)	NP_001337914.1:n.806-20735T>A
NR_033807.3:n.3158A>T (CYP3A5)