Canonical Allele Identifier: CA1729180875

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768396_99768397delinsGC , CM000669.2:g.99768396_99768397delinsGC	GRCh38
NC_000007.13:g.99366019_99366020delinsGC , CM000669.1:g.99366019_99366020delinsGC	GRCh37
NC_000007.12:g.99203955_99203956delinsGC	NCBI36
NG_008421.1:g.20789_20790delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.627_628delinsGC	ENSP00000337915.3:p.Lys209=
ENST00000651514.1:c.627_628delinsGC MANE Select	ENSP00000498939.1:p.Lys209=
ENST00000651783.1:c.168_169delinsGC	ENSP00000498924.1:p.Lys56=
ENST00000652018.1:c.480_481delinsGC	ENSP00000498733.1:p.Lys160=
ENST00000336411.6:c.627_628delinsGC	ENSP00000337915.2:p.Lys209=
ENST00000354593.6:c.177_178delinsGC	ENSP00000346607.2:p.Lys59=
NM_001202855.2:c.627_628delinsGC	NP_001189784.1:p.Lys209=
NM_017460.5:c.627_628delinsGC	NP_059488.2:p.Lys209=
XM_011515841.1:c.627_628delinsGC	XP_011514143.1:p.Lys209=
XM_011515842.1:c.627_628delinsGC	XP_011514144.1:p.Lys209=
NM_017460.6:c.627_628delinsGC MANE Select	NP_059488.2:p.Lys209=
NM_001202855.3:c.627_628delinsGC	NP_001189784.1:p.Lys209=