Canonical Allele Identifier: CA1729216977
Gene: CYP3A7 HGNC NCBI
CYP3A7-CYP3A51P HGNC NCBI
ZSCAN25 HGNC NCBI

Linked Data

dbSNP Id: rs10211
gnomAD v4: 7-99705371-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99705371T>A , CM000669.2:g.99705371T>A GRCh38
NG_007983.1:g.34828A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000336374.4:c.*129A>T (CYP3A7) MANE Select ENSP00000337450.2:n.*129A>T
ENST00000620220.6:c.1416+2441A>T (CYP3A7-CYP3A51P) ENSP00000479282.3:n.1416+2441A>T
ENST00000336374.3:c.*129A>T (CYP3A7) ENSP00000337450.2:n.*129A>T
ENST00000477357.5:n.1980A>T (CYP3A7)
ENST00000611620.4:c.1497+144A>T (CYP3A7-CYP3A51P) ENSP00000480571.1:n.1497+144A>T
ENST00000620220.4:c.1416+2441A>T (CYP3A7-CYP3A51P) ENSP00000479282.1:n.1416+2441A>T
NM_000765.4:c.*129A>T (CYP3A7) NP_000756.3:n.*129A>T
NM_001256497.2:c.1497+144A>T (CYP3A7-CYP3A51P) NP_001243426.2:n.1497+144A>T
XR_927402.1:n.1467-18104T>A (ZSCAN25)
XR_927402.2:n.1466-18104T>A (ZSCAN25)
NM_000765.5:c.*129A>T (CYP3A7) MANE Select NP_000756.3:n.*129A>T
NM_001256497.3:c.1497+144A>T (CYP3A7-CYP3A51P) NP_001243426.2:n.1497+144A>T