Canonical Allele Identifier: CA1104975775

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1815298204
• gnomAD v3: 7-99760757-TACAG-T
• gnomAD v4: 7-99760757-TACAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760760_99760763del , CM000669.2:g.99760760_99760763del	GRCh38
NC_000007.13:g.99358383_99358386del , CM000669.1:g.99358383_99358386del	GRCh37
NC_000007.12:g.99196319_99196322del	NCBI36
NG_008421.1:g.28425_28428del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1509+58_1509+61del	ENSP00000337915.3:n.1509+58_1509+61del
ENST00000651162.1:n.851+58_851+61del
ENST00000651514.1:c.1416+58_1416+61del MANE Select	ENSP00000498939.1:n.1416+58_1416+61del
ENST00000651783.1:c.957+58_957+61del	ENSP00000498924.1:n.957+58_957+61del
ENST00000652018.1:c.1269+58_1269+61del	ENSP00000498733.1:n.1269+58_1269+61del
ENST00000336411.6:c.1416+58_1416+61del	ENSP00000337915.2:n.1416+58_1416+61del
ENST00000354593.6:c.966+58_966+61del	ENSP00000346607.2:n.966+58_966+61del
NM_001202855.2:c.1413+58_1413+61del	NP_001189784.1:n.1413+58_1413+61del
NM_017460.5:c.1416+58_1416+61del	NP_059488.2:n.1416+58_1416+61del
XM_011515841.1:c.1509+58_1509+61del	XP_011514143.1:n.1509+58_1509+61del
XM_011515842.1:c.1506+58_1506+61del	XP_011514144.1:n.1506+58_1506+61del
NM_017460.6:c.1416+58_1416+61del MANE Select	NP_059488.2:n.1416+58_1416+61del
NM_001202855.3:c.1413+58_1413+61del	NP_001189784.1:n.1413+58_1413+61del