Canonical Allele Identifier: CA2578954351
Gene: CYP3A5 HGNC NCBI
ZSCAN25 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99648299A>G , CM000669.2:g.99648299A>G GRCh38
NC_000007.13:g.99245922A>G , CM000669.1:g.99245922A>G GRCh37
NC_000007.12:g.99083858A>G NCBI36
NG_007938.1:g.36700T>C
NG_007938.2:g.36700T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000646887.1:c.*1200T>C (CYP3A5) ENSP00000496704.1:n.*1200T>C
ENST00000222982.8:c.*6T>C (CYP3A5) MANE Select ENSP00000222982.4:n.*6T>C
ENST00000339843.6:c.*2999T>C (CYP3A5) ENSP00000343074.2:n.*2999T>C
ENST00000461920.5:n.2107T>C (CYP3A5)
ENST00000469887.5:n.3048T>C (CYP3A5)
NM_000777.4:c.*6T>C (CYP3A5) NP_000768.1:n.*6T>C
NM_001291829.1:c.*6T>C (CYP3A5) NP_001278758.1:n.*6T>C
NM_001291830.1:c.*6T>C (CYP3A5) NP_001278759.1:n.*6T>C
NR_033807.2:n.3249T>C (CYP3A5)
XM_011515843.1:c.*6T>C (CYP3A5) XP_011514145.1:n.*6T>C
XM_011515844.1:c.*6T>C (CYP3A5) XP_011514146.1:n.*6T>C
XM_011515845.1:c.*6T>C (CYP3A5) XP_011514147.1:n.*6T>C
XM_011515846.1:c.*6T>C (CYP3A5) XP_011514148.1:n.*6T>C
XM_011515847.1:c.*6T>C (CYP3A5) XP_011514149.1:n.*6T>C
XM_011515909.1:c.806-20796A>G (ZSCAN25) XP_011514211.1:n.806-20796A>G
XR_927402.1:n.1466+24119A>G (ZSCAN25)
NM_000777.5:c.*6T>C (CYP3A5) MANE Select NP_000768.1:n.*6T>C
NM_001350984.1:c.806-20796A>G (ZSCAN25) NP_001337913.1:n.806-20796A>G
NM_001350985.1:c.806-20796A>G (ZSCAN25) NP_001337914.1:n.806-20796A>G
XM_011515909.2:c.806-20796A>G (ZSCAN25) XP_011514211.1:n.806-20796A>G
XR_927402.2:n.1465+24119A>G (ZSCAN25)
NM_001291829.2:c.*6T>C (CYP3A5) NP_001278758.1:n.*6T>C
NM_001291830.2:c.*6T>C (CYP3A5) NP_001278759.1:n.*6T>C
NM_001350984.2:c.806-20796A>G (ZSCAN25) NP_001337913.1:n.806-20796A>G
NM_001350985.2:c.806-20796A>G (ZSCAN25) NP_001337914.1:n.806-20796A>G
NR_033807.3:n.3219T>C (CYP3A5)