Canonical Allele Identifier: CA1729180865

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768376_99768379delinsCAAA , CM000669.2:g.99768376_99768379delinsCAAA	GRCh38
NC_000007.13:g.99365999_99366002delinsCAAA , CM000669.1:g.99365999_99366002delinsCAAA	GRCh37
NC_000007.12:g.99203935_99203938delinsCAAA	NCBI36
NG_008421.1:g.20807_20810delinsTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.645_648delinsTTTG	ENSP00000337915.3:p.Phe215=
ENST00000651514.1:c.645_648delinsTTTG MANE Select	ENSP00000498939.1:p.Phe215=
ENST00000651783.1:c.186_189delinsTTTG	ENSP00000498924.1:p.Phe62=
ENST00000652018.1:c.498_501delinsTTTG	ENSP00000498733.1:p.Phe166=
ENST00000336411.6:c.645_648delinsTTTG	ENSP00000337915.2:p.Phe215=
ENST00000354593.6:c.195_198delinsTTTG	ENSP00000346607.2:p.Phe65=
NM_001202855.2:c.645_648delinsTTTG	NP_001189784.1:p.Phe215=
NM_017460.5:c.645_648delinsTTTG	NP_059488.2:p.Phe215=
XM_011515841.1:c.645_648delinsTTTG	XP_011514143.1:p.Phe215=
XM_011515842.1:c.645_648delinsTTTG	XP_011514144.1:p.Phe215=
NM_017460.6:c.645_648delinsTTTG MANE Select	NP_059488.2:p.Phe215=
NM_001202855.3:c.645_648delinsTTTG	NP_001189784.1:p.Phe215=