Canonical Allele Identifier: CA163129606
Gene: CYP3A7 HGNC NCBI
CYP3A7-CYP3A51P HGNC NCBI
ZSCAN25 HGNC NCBI
MyVariant.info:
GRCh38 chr7:g.99705371T>C
gnomAD v3:
7:99705371 T / C
gnomAD v4:
chr7-99705371-T-C
Joint Max Group AF 0.58698798 (AFR)
Genomes Max Group AF 0.57933931 (AFR)
Exomes Max Group AF 0.59532932 (AFR)
dbSNP:
10211
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Genomic Alleles

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

Transcript Alleles

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