Canonical Allele Identifier: CA1729216921
Gene: CYP3A7 HGNC NCBI
CYP3A7-CYP3A51P HGNC NCBI
ZSCAN25 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99705310T= , CM000669.2:g.99705310T= GRCh38
NC_000007.13:g.99302933T= , CM000669.1:g.99302933T= GRCh37
NC_000007.12:g.99140869T= NCBI36
NG_007983.1:g.34889A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336374.4:c.*190A= (CYP3A7) MANE Select ENSP00000337450.2:n.*190A=
ENST00000620220.6:c.1416+2502A= (CYP3A7-CYP3A51P) ENSP00000479282.3:n.1416+2502A=
ENST00000336374.3:c.*190A= (CYP3A7) ENSP00000337450.2:n.*190A=
ENST00000477357.5:n.2041A= (CYP3A7)
ENST00000611620.4:c.1497+205A= (CYP3A7-CYP3A51P) ENSP00000480571.1:n.1497+205A=
ENST00000620220.4:c.1416+2502A= (CYP3A7-CYP3A51P) ENSP00000479282.1:n.1416+2502A=
NM_000765.4:c.*190A= (CYP3A7) NP_000756.3:n.*190A=
NM_001256497.2:c.1497+205A= (CYP3A7-CYP3A51P) NP_001243426.2:n.1497+205A=
XR_927402.1:n.1467-18165T= (ZSCAN25)
XR_927402.2:n.1466-18165T= (ZSCAN25)
NM_000765.5:c.*190A= (CYP3A7) MANE Select NP_000756.3:n.*190A=
NM_001256497.3:c.1497+205A= (CYP3A7-CYP3A51P) NP_001243426.2:n.1497+205A=