Canonical Allele Identifier: CA1729216902

Gene: CYP3A7 CYP3A7-CYP3A51P ZSCAN25

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99705277A= , CM000669.2:g.99705277A=	GRCh38
NC_000007.13:g.99302900A= , CM000669.1:g.99302900A=	GRCh37
NC_000007.12:g.99140836A=	NCBI36
NG_007983.1:g.34922T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336374.4:c.*223T= (CYP3A7) MANE Select	ENSP00000337450.2:n.*223T=
ENST00000620220.6:c.1416+2535T= (CYP3A7-CYP3A51P)	ENSP00000479282.3:n.1416+2535T=
ENST00000336374.3:c.*223T= (CYP3A7)	ENSP00000337450.2:n.*223T=
ENST00000477357.5:n.2074T= (CYP3A7)
ENST00000611620.4:c.1497+238T= (CYP3A7-CYP3A51P)	ENSP00000480571.1:n.1497+238T=
ENST00000620220.4:c.1416+2535T= (CYP3A7-CYP3A51P)	ENSP00000479282.1:n.1416+2535T=
NM_000765.4:c.*223T= (CYP3A7)	NP_000756.3:n.*223T=
NM_001256497.2:c.1497+238T= (CYP3A7-CYP3A51P)	NP_001243426.2:n.1497+238T=
XR_927402.1:n.1467-18198A= (ZSCAN25)
XR_927402.2:n.1466-18198A= (ZSCAN25)
NM_000765.5:c.*223T= (CYP3A7) MANE Select	NP_000756.3:n.*223T=
NM_001256497.3:c.1497+238T= (CYP3A7-CYP3A51P)	NP_001243426.2:n.1497+238T=