Canonical Allele Identifier: CA576402045

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1268187525
• gnomAD v2: 7-99366979-CAA-C
• gnomAD v3: 7-99769356-CAA-C
• gnomAD v4: 7-99769356-CAA-C
• MyVariant Identifiers: chr7:g.99366980_99366981del (hg19) ; chr7:g.99769357_99769358del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769358_99769359del , CM000669.2:g.99769358_99769359del	GRCh38
NC_000007.13:g.99366981_99366982del , CM000669.1:g.99366981_99366982del	GRCh37
NC_000007.12:g.99204917_99204918del	NCBI36
NG_008421.1:g.19828_19829del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.521+410_521+411del	ENSP00000337915.3:n.521+410_521+411del
ENST00000651514.1:c.521+410_521+411del MANE Select	ENSP00000498939.1:n.521+410_521+411del
ENST00000651783.1:c.58-851_58-850del	ENSP00000498924.1:n.58-851_58-850del
ENST00000652018.1:c.374+410_374+411del	ENSP00000498733.1:n.374+410_374+411del
ENST00000336411.6:c.521+410_521+411del	ENSP00000337915.2:n.521+410_521+411del
ENST00000354593.6:c.72-856_72-855del	ENSP00000346607.2:n.72-856_72-855del
NM_001202855.2:c.521+410_521+411del	NP_001189784.1:n.521+410_521+411del
NM_017460.5:c.521+410_521+411del	NP_059488.2:n.521+410_521+411del
XM_011515841.1:c.521+410_521+411del	XP_011514143.1:n.521+410_521+411del
XM_011515842.1:c.521+410_521+411del	XP_011514144.1:n.521+410_521+411del
NM_017460.6:c.521+410_521+411del MANE Select	NP_059488.2:n.521+410_521+411del
NM_001202855.3:c.521+410_521+411del	NP_001189784.1:n.521+410_521+411del