Canonical Allele Identifier: CA2683981898
Gene: CYP3A7 HGNC NCBI
CYP3A7-CYP3A51P HGNC NCBI
ZSCAN25 HGNC NCBI

Linked Data

gnomAD v4: 7-99705307-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99705307C>A , CM000669.2:g.99705307C>A GRCh38
NC_000007.13:g.99302930C>A , CM000669.1:g.99302930C>A GRCh37
NC_000007.12:g.99140866C>A NCBI36
NG_007983.1:g.34892G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000336374.4:c.*193G>T (CYP3A7) MANE Select ENSP00000337450.2:n.*193G>T
ENST00000620220.6:c.1416+2505G>T (CYP3A7-CYP3A51P) ENSP00000479282.3:n.1416+2505G>T
ENST00000336374.3:c.*193G>T (CYP3A7) ENSP00000337450.2:n.*193G>T
ENST00000477357.5:n.2044G>T (CYP3A7)
ENST00000611620.4:c.1497+208G>T (CYP3A7-CYP3A51P) ENSP00000480571.1:n.1497+208G>T
ENST00000620220.4:c.1416+2505G>T (CYP3A7-CYP3A51P) ENSP00000479282.1:n.1416+2505G>T
NM_000765.4:c.*193G>T (CYP3A7) NP_000756.3:n.*193G>T
NM_001256497.2:c.1497+208G>T (CYP3A7-CYP3A51P) NP_001243426.2:n.1497+208G>T
XR_927402.1:n.1467-18168C>A (ZSCAN25)
XR_927402.2:n.1466-18168C>A (ZSCAN25)
NM_000765.5:c.*193G>T (CYP3A7) MANE Select NP_000756.3:n.*193G>T
NM_001256497.3:c.1497+208G>T (CYP3A7-CYP3A51P) NP_001243426.2:n.1497+208G>T
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