Canonical Allele Identifier: CA368365622
Gene: CYP3A5 HGNC NCBI
ZSCAN25 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99665246T>G , CM000669.2:g.99665246T>G GRCh38
NC_000007.13:g.99262869T>G , CM000669.1:g.99262869T>G GRCh37
NC_000007.12:g.99100805T>G NCBI36
NG_007938.1:g.19753A>C
NG_007938.2:g.19753A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000646887.1:c.*275A>C (CYP3A5) ENSP00000496704.1:n.*275A>C
ENST00000222982.8:c.590A>C (CYP3A5) MANE Select ENSP00000222982.4:p.Asn197Thr
ENST00000339843.6:c.*989A>C (CYP3A5) ENSP00000343074.2:n.*989A>C
ENST00000461920.5:n.1182A>C (CYP3A5)
ENST00000463364.5:n.909A>C (CYP3A5)
ENST00000466061.5:n.930A>C (CYP3A5)
ENST00000469887.5:n.1038A>C (CYP3A5)
ENST00000481825.5:n.1190A>C (CYP3A5)
NM_000777.4:c.590A>C (CYP3A5) NP_000768.1:p.Asn197Thr
NM_001291829.1:c.251A>C (CYP3A5) NP_001278758.1:p.Asn84Thr
NM_001291830.1:c.560A>C (CYP3A5) NP_001278759.1:p.Asn187Thr
NR_033807.2:n.1239A>C (CYP3A5)
XM_006715859.2:c.590A>C (CYP3A5) XP_006715922.1:p.Asn197Thr
XM_011515843.1:c.251A>C (CYP3A5) XP_011514145.1:p.Asn84Thr
XM_011515844.1:c.251A>C (CYP3A5) XP_011514146.1:p.Asn84Thr
XM_011515845.1:c.50A>C (CYP3A5) XP_011514147.1:p.Asn17Thr
XM_011515846.1:c.50A>C (CYP3A5) XP_011514148.1:p.Asn17Thr
XM_011515847.1:c.50A>C (CYP3A5) XP_011514149.1:p.Asn17Thr
XM_011515909.1:c.806-3849T>G (ZSCAN25) XP_011514211.1:n.806-3849T>G
XR_927402.1:n.1466+41066T>G (ZSCAN25)
NM_000777.5:c.590A>C (CYP3A5) MANE Select NP_000768.1:p.Asn197Thr
NM_001350984.1:c.806-3849T>G (ZSCAN25) NP_001337913.1:n.806-3849T>G
NM_001350985.1:c.806-3849T>G (ZSCAN25) NP_001337914.1:n.806-3849T>G
XM_011515909.2:c.806-3849T>G (ZSCAN25) XP_011514211.1:n.806-3849T>G
XR_927402.2:n.1465+41066T>G (ZSCAN25)
NM_001291829.2:c.251A>C (CYP3A5) NP_001278758.1:p.Asn84Thr
NM_001291830.2:c.560A>C (CYP3A5) NP_001278759.1:p.Asn187Thr
NM_001350984.2:c.806-3849T>G (ZSCAN25) NP_001337913.1:n.806-3849T>G
NM_001350985.2:c.806-3849T>G (ZSCAN25) NP_001337914.1:n.806-3849T>G
NR_033807.3:n.1209A>C (CYP3A5)