Canonical Allele Identifier: CA368365673
Gene: CYP3A5 HGNC NCBI
ZSCAN25 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99665261T>G , CM000669.2:g.99665261T>G GRCh38
NC_000007.13:g.99262884T>G , CM000669.1:g.99262884T>G GRCh37
NC_000007.12:g.99100820T>G NCBI36
NG_007938.1:g.19738A>C
NG_007938.2:g.19738A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000646887.1:c.*260A>C (CYP3A5) ENSP00000496704.1:n.*260A>C
ENST00000222982.8:c.575A>C (CYP3A5) MANE Select ENSP00000222982.4:p.Asn192Thr
ENST00000339843.6:c.*974A>C (CYP3A5) ENSP00000343074.2:n.*974A>C
ENST00000461920.5:n.1167A>C (CYP3A5)
ENST00000463364.5:n.894A>C (CYP3A5)
ENST00000466061.5:n.915A>C (CYP3A5)
ENST00000469887.5:n.1023A>C (CYP3A5)
ENST00000481825.5:n.1175A>C (CYP3A5)
NM_000777.4:c.575A>C (CYP3A5) NP_000768.1:p.Asn192Thr
NM_001291829.1:c.236A>C (CYP3A5) NP_001278758.1:p.Asn79Thr
NM_001291830.1:c.545A>C (CYP3A5) NP_001278759.1:p.Asn182Thr
NR_033807.2:n.1224A>C (CYP3A5)
XM_006715859.2:c.575A>C (CYP3A5) XP_006715922.1:p.Asn192Thr
XM_011515843.1:c.236A>C (CYP3A5) XP_011514145.1:p.Asn79Thr
XM_011515844.1:c.236A>C (CYP3A5) XP_011514146.1:p.Asn79Thr
XM_011515845.1:c.35A>C (CYP3A5) XP_011514147.1:p.Asn12Thr
XM_011515846.1:c.35A>C (CYP3A5) XP_011514148.1:p.Asn12Thr
XM_011515847.1:c.35A>C (CYP3A5) XP_011514149.1:p.Asn12Thr
XM_011515909.1:c.806-3834T>G (ZSCAN25) XP_011514211.1:n.806-3834T>G
XR_927402.1:n.1466+41081T>G (ZSCAN25)
NM_000777.5:c.575A>C (CYP3A5) MANE Select NP_000768.1:p.Asn192Thr
NM_001350984.1:c.806-3834T>G (ZSCAN25) NP_001337913.1:n.806-3834T>G
NM_001350985.1:c.806-3834T>G (ZSCAN25) NP_001337914.1:n.806-3834T>G
XM_011515909.2:c.806-3834T>G (ZSCAN25) XP_011514211.1:n.806-3834T>G
XR_927402.2:n.1465+41081T>G (ZSCAN25)
NM_001291829.2:c.236A>C (CYP3A5) NP_001278758.1:p.Asn79Thr
NM_001291830.2:c.545A>C (CYP3A5) NP_001278759.1:p.Asn182Thr
NM_001350984.2:c.806-3834T>G (ZSCAN25) NP_001337913.1:n.806-3834T>G
NM_001350985.2:c.806-3834T>G (ZSCAN25) NP_001337914.1:n.806-3834T>G
NR_033807.3:n.1194A>C (CYP3A5)