Canonical Allele Identifier: CA844514431

Gene: CYP3A4

Linked Data

• dbSNP Id: rs768320602
• MyVariant Identifiers: chr7:g.99366000_99366002del (hg19) ; chr7:g.99768377_99768379del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768380_99768382del , CM000669.2:g.99768380_99768382del	GRCh38
NC_000007.13:g.99366003_99366005del , CM000669.1:g.99366003_99366005del	GRCh37
NC_000007.12:g.99203939_99203941del	NCBI36
NG_008421.1:g.20807_20809del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.645_647del	ENSP00000337915.3:p.Phe215del
ENST00000651514.1:c.645_647del MANE Select	ENSP00000498939.1:p.Phe215del
ENST00000651783.1:c.186_188del	ENSP00000498924.1:p.Phe62del
ENST00000652018.1:c.498_500del	ENSP00000498733.1:p.Phe166del
ENST00000336411.6:c.645_647del	ENSP00000337915.2:p.Phe215del
ENST00000354593.6:c.195_197del	ENSP00000346607.2:p.Phe65del
NM_001202855.2:c.645_647del	NP_001189784.1:p.Phe215del
NM_017460.5:c.645_647del	NP_059488.2:p.Phe215del
XM_011515841.1:c.645_647del	XP_011514143.1:p.Phe215del
XM_011515842.1:c.645_647del	XP_011514144.1:p.Phe215del
NM_017460.6:c.645_647del MANE Select	NP_059488.2:p.Phe215del
NM_001202855.3:c.645_647del	NP_001189784.1:p.Phe215del