Canonical Allele Identifier: CA844514040

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1443423007
• MyVariant Identifiers: chr7:g.99365244_99365246del (hg19) ; chr7:g.99767621_99767623del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767624_99767626del , CM000669.2:g.99767624_99767626del	GRCh38
NC_000007.13:g.99365247_99365249del , CM000669.1:g.99365247_99365249del	GRCh37
NC_000007.12:g.99203183_99203185del	NCBI36
NG_008421.1:g.21563_21565del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.671-365_671-363del	ENSP00000337915.3:n.671-365_671-363del
ENST00000651162.1:n.105+95_105+97del
ENST00000651514.1:c.671-365_671-363del MANE Select	ENSP00000498939.1:n.671-365_671-363del
ENST00000651783.1:c.212-365_212-363del	ENSP00000498924.1:n.212-365_212-363del
ENST00000652018.1:c.524-365_524-363del	ENSP00000498733.1:n.524-365_524-363del
ENST00000336411.6:c.671-365_671-363del	ENSP00000337915.2:n.671-365_671-363del
ENST00000354593.6:c.221-365_221-363del	ENSP00000346607.2:n.221-365_221-363del
NM_001202855.2:c.671-368_671-366del	NP_001189784.1:n.671-368_671-366del
NM_017460.5:c.671-365_671-363del	NP_059488.2:n.671-365_671-363del
XM_011515841.1:c.671-365_671-363del	XP_011514143.1:n.671-365_671-363del
XM_011515842.1:c.671-368_671-366del	XP_011514144.1:n.671-368_671-366del
NM_017460.6:c.671-365_671-363del MANE Select	NP_059488.2:n.671-365_671-363del
NM_001202855.3:c.671-368_671-366del	NP_001189784.1:n.671-368_671-366del