Canonical Allele Identifier: CA4368979
Gene: CYP3A7 HGNC NCBI
CYP3A7-CYP3A51P HGNC NCBI
ZSCAN25 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99709062G= , CM000669.2:g.99709062G= GRCh38
NG_007983.1:g.31137C=

Transcript Alleles

HGVS Amino-acid Change
NM_000765.5:c.1226C= (CYP3A7) MANE Select NP_000756.3:p.Thr409=
ENST00000336374.4:c.1226C= (CYP3A7) MANE Select ENSP00000337450.2:p.Thr409=
NM_000765.4:c.1226C= (CYP3A7) NP_000756.3:p.Thr409=
NM_001256497.2:c.1226C= (CYP3A7-CYP3A51P) NP_001243426.2:p.Thr409=
NM_001256497.3:c.1226C= (CYP3A7-CYP3A51P) NP_001243426.2:p.Thr409=
ENST00000336374.3:c.1226C= (CYP3A7) ENSP00000337450.2:p.Thr409=
ENST00000477357.5:n.1565C= (CYP3A7)
ENST00000611620.4:c.1226C= (CYP3A7-CYP3A51P) ENSP00000480571.1:p.Thr409=
ENST00000620220.4:c.1226C= (CYP3A7-CYP3A51P) ENSP00000479282.1:p.Thr409=
ENST00000620220.6:c.1226C= (CYP3A7-CYP3A51P) ENSP00000479282.3:p.Thr409=
XR_927402.1:n.1467-14413G= (ZSCAN25)
XR_927402.2:n.1466-14413G= (ZSCAN25)