Canonical Allele Identifier: CA1729216904
Gene: CYP3A7 HGNC NCBI
CYP3A7-CYP3A51P HGNC NCBI
ZSCAN25 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99705283C= , CM000669.2:g.99705283C= GRCh38
NC_000007.13:g.99302906C= , CM000669.1:g.99302906C= GRCh37
NC_000007.12:g.99140842C= NCBI36
NG_007983.1:g.34916G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336374.4:c.*217G= (CYP3A7) MANE Select ENSP00000337450.2:n.*217G=
ENST00000620220.6:c.1416+2529G= (CYP3A7-CYP3A51P) ENSP00000479282.3:n.1416+2529G=
ENST00000336374.3:c.*217G= (CYP3A7) ENSP00000337450.2:n.*217G=
ENST00000477357.5:n.2068G= (CYP3A7)
ENST00000611620.4:c.1497+232G= (CYP3A7-CYP3A51P) ENSP00000480571.1:n.1497+232G=
ENST00000620220.4:c.1416+2529G= (CYP3A7-CYP3A51P) ENSP00000479282.1:n.1416+2529G=
NM_000765.4:c.*217G= (CYP3A7) NP_000756.3:n.*217G=
NM_001256497.2:c.1497+232G= (CYP3A7-CYP3A51P) NP_001243426.2:n.1497+232G=
XR_927402.1:n.1467-18192C= (ZSCAN25)
XR_927402.2:n.1466-18192C= (ZSCAN25)
NM_000765.5:c.*217G= (CYP3A7) MANE Select NP_000756.3:n.*217G=
NM_001256497.3:c.1497+232G= (CYP3A7-CYP3A51P) NP_001243426.2:n.1497+232G=