Canonical Allele Identifier: CA576410718
Gene: CYP3A5 HGNC NCBI
ZSCAN25 HGNC NCBI

Linked Data

dbSNP Id: rs1341136835
gnomAD v2: 7-99245886-C-A
gnomAD v4: 7-99648263-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99648263C>A , CM000669.2:g.99648263C>A GRCh38
NC_000007.13:g.99245886C>A , CM000669.1:g.99245886C>A GRCh37
NC_000007.12:g.99083822C>A NCBI36
NG_007938.1:g.36736G>T
NG_007938.2:g.36736G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000646887.1:c.*1236G>T (CYP3A5) ENSP00000496704.1:n.*1236G>T
ENST00000222982.8:c.*42G>T (CYP3A5) MANE Select ENSP00000222982.4:n.*42G>T
ENST00000339843.6:c.*3035G>T (CYP3A5) ENSP00000343074.2:n.*3035G>T
ENST00000461920.5:n.2143G>T (CYP3A5)
ENST00000469887.5:n.3084G>T (CYP3A5)
NM_000777.4:c.*42G>T (CYP3A5) NP_000768.1:n.*42G>T
NM_001291829.1:c.*42G>T (CYP3A5) NP_001278758.1:n.*42G>T
NM_001291830.1:c.*42G>T (CYP3A5) NP_001278759.1:n.*42G>T
NR_033807.2:n.3285G>T (CYP3A5)
XM_011515843.1:c.*42G>T (CYP3A5) XP_011514145.1:n.*42G>T
XM_011515844.1:c.*42G>T (CYP3A5) XP_011514146.1:n.*42G>T
XM_011515845.1:c.*42G>T (CYP3A5) XP_011514147.1:n.*42G>T
XM_011515846.1:c.*42G>T (CYP3A5) XP_011514148.1:n.*42G>T
XM_011515847.1:c.*42G>T (CYP3A5) XP_011514149.1:n.*42G>T
XM_011515909.1:c.806-20832C>A (ZSCAN25) XP_011514211.1:n.806-20832C>A
XM_011515910.1:c.*740C>A (ZSCAN25) XP_011514212.1:n.*740C>A
XR_927402.1:n.1466+24083C>A (ZSCAN25)
NM_000777.5:c.*42G>T (CYP3A5) MANE Select NP_000768.1:n.*42G>T
NM_001350984.1:c.806-20832C>A (ZSCAN25) NP_001337913.1:n.806-20832C>A
NM_001350985.1:c.806-20832C>A (ZSCAN25) NP_001337914.1:n.806-20832C>A
XM_011515909.2:c.806-20832C>A (ZSCAN25) XP_011514211.1:n.806-20832C>A
XR_927402.2:n.1465+24083C>A (ZSCAN25)
NM_001291829.2:c.*42G>T (CYP3A5) NP_001278758.1:n.*42G>T
NM_001291830.2:c.*42G>T (CYP3A5) NP_001278759.1:n.*42G>T
NM_001350984.2:c.806-20832C>A (ZSCAN25) NP_001337913.1:n.806-20832C>A
NM_001350985.2:c.806-20832C>A (ZSCAN25) NP_001337914.1:n.806-20832C>A
NR_033807.3:n.3255G>T (CYP3A5)