Canonical Allele Identifier: CA456685059
Gene: CYP3A5 HGNC NCBI
ZSCAN25 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.99245985T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99648362T>A , CM000669.2:g.99648362T>A GRCh38
NC_000007.13:g.99245985T>A , CM000669.1:g.99245985T>A GRCh37
NC_000007.12:g.99083921T>A NCBI36
NG_007938.1:g.36637A>T
NG_007938.2:g.36637A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000646887.1:c.*1137A>T (CYP3A5) ENSP00000496704.1:n.*1137A>T
ENST00000222982.8:c.1452A>T (CYP3A5) MANE Select ENSP00000222982.4:p.Pro484=
ENST00000339843.6:c.*2936A>T (CYP3A5) ENSP00000343074.2:n.*2936A>T
ENST00000461920.5:n.2044A>T (CYP3A5)
ENST00000469887.5:n.2985A>T (CYP3A5)
NM_000777.4:c.1452A>T (CYP3A5) NP_000768.1:p.Pro484=
NM_001291829.1:c.1113A>T (CYP3A5) NP_001278758.1:p.Pro371=
NM_001291830.1:c.1422A>T (CYP3A5) NP_001278759.1:p.Pro474=
NR_033807.2:n.3186A>T (CYP3A5)
XM_011515843.1:c.1113A>T (CYP3A5) XP_011514145.1:p.Pro371=
XM_011515844.1:c.1113A>T (CYP3A5) XP_011514146.1:p.Pro371=
XM_011515845.1:c.912A>T (CYP3A5) XP_011514147.1:p.Pro304=
XM_011515846.1:c.912A>T (CYP3A5) XP_011514148.1:p.Pro304=
XM_011515847.1:c.912A>T (CYP3A5) XP_011514149.1:p.Pro304=
XM_011515909.1:c.806-20733T>A (ZSCAN25) XP_011514211.1:n.806-20733T>A
XR_927402.1:n.1466+24182T>A (ZSCAN25)
NM_000777.5:c.1452A>T (CYP3A5) MANE Select NP_000768.1:p.Pro484=
NM_001350984.1:c.806-20733T>A (ZSCAN25) NP_001337913.1:n.806-20733T>A
NM_001350985.1:c.806-20733T>A (ZSCAN25) NP_001337914.1:n.806-20733T>A
XM_011515909.2:c.806-20733T>A (ZSCAN25) XP_011514211.1:n.806-20733T>A
XR_927402.2:n.1465+24182T>A (ZSCAN25)
NM_001291829.2:c.1113A>T (CYP3A5) NP_001278758.1:p.Pro371=
NM_001291830.2:c.1422A>T (CYP3A5) NP_001278759.1:p.Pro474=
NM_001350984.2:c.806-20733T>A (ZSCAN25) NP_001337913.1:n.806-20733T>A
NM_001350985.2:c.806-20733T>A (ZSCAN25) NP_001337914.1:n.806-20733T>A
NR_033807.3:n.3156A>T (CYP3A5)