Canonical Allele Identifier: CA456685029

Gene: CYP3A5 ZSCAN25

Linked Data

• gnomAD v4: 7-99648353-G-A
• MyVariant Identifiers: chr7:g.99245976G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99648353G>A , CM000669.2:g.99648353G>A	GRCh38
NC_000007.13:g.99245976G>A , CM000669.1:g.99245976G>A	GRCh37
NC_000007.12:g.99083912G>A	NCBI36
NG_007938.1:g.36646C>T
NG_007938.2:g.36646C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000646887.1:c.*1146C>T (CYP3A5)	ENSP00000496704.1:n.*1146C>T
ENST00000222982.8:c.1461C>T (CYP3A5) MANE Select	ENSP00000222982.4:p.Pro487=
ENST00000339843.6:c.*2945C>T (CYP3A5)	ENSP00000343074.2:n.*2945C>T
ENST00000461920.5:n.2053C>T (CYP3A5)
ENST00000469887.5:n.2994C>T (CYP3A5)
NM_000777.4:c.1461C>T (CYP3A5)	NP_000768.1:p.Pro487=
NM_001291829.1:c.1122C>T (CYP3A5)	NP_001278758.1:p.Pro374=
NM_001291830.1:c.1431C>T (CYP3A5)	NP_001278759.1:p.Pro477=
NR_033807.2:n.3195C>T (CYP3A5)
XM_011515843.1:c.1122C>T (CYP3A5)	XP_011514145.1:p.Pro374=
XM_011515844.1:c.1122C>T (CYP3A5)	XP_011514146.1:p.Pro374=
XM_011515845.1:c.921C>T (CYP3A5)	XP_011514147.1:p.Pro307=
XM_011515846.1:c.921C>T (CYP3A5)	XP_011514148.1:p.Pro307=
XM_011515847.1:c.921C>T (CYP3A5)	XP_011514149.1:p.Pro307=
XM_011515909.1:c.806-20742G>A (ZSCAN25)	XP_011514211.1:n.806-20742G>A
XR_927402.1:n.1466+24173G>A (ZSCAN25)
NM_000777.5:c.1461C>T (CYP3A5) MANE Select	NP_000768.1:p.Pro487=
NM_001350984.1:c.806-20742G>A (ZSCAN25)	NP_001337913.1:n.806-20742G>A
NM_001350985.1:c.806-20742G>A (ZSCAN25)	NP_001337914.1:n.806-20742G>A
XM_011515909.2:c.806-20742G>A (ZSCAN25)	XP_011514211.1:n.806-20742G>A
XR_927402.2:n.1465+24173G>A (ZSCAN25)
NM_001291829.2:c.1122C>T (CYP3A5)	NP_001278758.1:p.Pro374=
NM_001291830.2:c.1431C>T (CYP3A5)	NP_001278759.1:p.Pro477=
NM_001350984.2:c.806-20742G>A (ZSCAN25)	NP_001337913.1:n.806-20742G>A
NM_001350985.2:c.806-20742G>A (ZSCAN25)	NP_001337914.1:n.806-20742G>A
NR_033807.3:n.3165C>T (CYP3A5)