Canonical Allele Identifier: CA368365655
Gene: CYP3A5 HGNC NCBI
ZSCAN25 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99665256C>A , CM000669.2:g.99665256C>A GRCh38
NC_000007.13:g.99262879C>A , CM000669.1:g.99262879C>A GRCh37
NC_000007.12:g.99100815C>A NCBI36
NG_007938.1:g.19743G>T
NG_007938.2:g.19743G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000646887.1:c.*265G>T (CYP3A5) ENSP00000496704.1:n.*265G>T
ENST00000222982.8:c.580G>T (CYP3A5) MANE Select ENSP00000222982.4:p.Asp194Tyr
ENST00000339843.6:c.*979G>T (CYP3A5) ENSP00000343074.2:n.*979G>T
ENST00000461920.5:n.1172G>T (CYP3A5)
ENST00000463364.5:n.899G>T (CYP3A5)
ENST00000466061.5:n.920G>T (CYP3A5)
ENST00000469887.5:n.1028G>T (CYP3A5)
ENST00000481825.5:n.1180G>T (CYP3A5)
NM_000777.4:c.580G>T (CYP3A5) NP_000768.1:p.Asp194Tyr
NM_001291829.1:c.241G>T (CYP3A5) NP_001278758.1:p.Asp81Tyr
NM_001291830.1:c.550G>T (CYP3A5) NP_001278759.1:p.Asp184Tyr
NR_033807.2:n.1229G>T (CYP3A5)
XM_006715859.2:c.580G>T (CYP3A5) XP_006715922.1:p.Asp194Tyr
XM_011515843.1:c.241G>T (CYP3A5) XP_011514145.1:p.Asp81Tyr
XM_011515844.1:c.241G>T (CYP3A5) XP_011514146.1:p.Asp81Tyr
XM_011515845.1:c.40G>T (CYP3A5) XP_011514147.1:p.Asp14Tyr
XM_011515846.1:c.40G>T (CYP3A5) XP_011514148.1:p.Asp14Tyr
XM_011515847.1:c.40G>T (CYP3A5) XP_011514149.1:p.Asp14Tyr
XM_011515909.1:c.806-3839C>A (ZSCAN25) XP_011514211.1:n.806-3839C>A
XR_927402.1:n.1466+41076C>A (ZSCAN25)
NM_000777.5:c.580G>T (CYP3A5) MANE Select NP_000768.1:p.Asp194Tyr
NM_001350984.1:c.806-3839C>A (ZSCAN25) NP_001337913.1:n.806-3839C>A
NM_001350985.1:c.806-3839C>A (ZSCAN25) NP_001337914.1:n.806-3839C>A
XM_011515909.2:c.806-3839C>A (ZSCAN25) XP_011514211.1:n.806-3839C>A
XR_927402.2:n.1465+41076C>A (ZSCAN25)
NM_001291829.2:c.241G>T (CYP3A5) NP_001278758.1:p.Asp81Tyr
NM_001291830.2:c.550G>T (CYP3A5) NP_001278759.1:p.Asp184Tyr
NM_001350984.2:c.806-3839C>A (ZSCAN25) NP_001337913.1:n.806-3839C>A
NM_001350985.2:c.806-3839C>A (ZSCAN25) NP_001337914.1:n.806-3839C>A
NR_033807.3:n.1199G>T (CYP3A5)