Canonical Allele Identifier: CA1104978564

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1815524426
• gnomAD v3: 7-99768221-CAT-C
• gnomAD v4: 7-99768221-CAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768224_99768225del , CM000669.2:g.99768224_99768225del	GRCh38
NC_000007.13:g.99365847_99365848del , CM000669.1:g.99365847_99365848del	GRCh37
NC_000007.12:g.99203783_99203784del	NCBI36
NG_008421.1:g.20963_20964del

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.670+131_670+132del	ENSP00000337915.3:n.670+131_670+132del
ENST00000651514.1:c.670+131_670+132del MANE Select	ENSP00000498939.1:n.670+131_670+132del
ENST00000651783.1:c.211+131_211+132del	ENSP00000498924.1:n.211+131_211+132del
ENST00000652018.1:c.523+131_523+132del	ENSP00000498733.1:n.523+131_523+132del
ENST00000336411.6:c.670+131_670+132del	ENSP00000337915.2:n.670+131_670+132del
ENST00000354593.6:c.220+131_220+132del	ENSP00000346607.2:n.220+131_220+132del
NM_001202855.2:c.670+131_670+132del	NP_001189784.1:n.670+131_670+132del
NM_017460.5:c.670+131_670+132del	NP_059488.2:n.670+131_670+132del
XM_011515841.1:c.670+131_670+132del	XP_011514143.1:n.670+131_670+132del
XM_011515842.1:c.670+131_670+132del	XP_011514144.1:n.670+131_670+132del
NM_017460.6:c.670+131_670+132del MANE Select	NP_059488.2:n.670+131_670+132del
NM_001202855.3:c.670+131_670+132del	NP_001189784.1:n.670+131_670+132del