Canonical Allele Identifier: CA1729180737

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768141_99768143delinsCAG , CM000669.2:g.99768141_99768143delinsCAG	GRCh38
NC_000007.13:g.99365764_99365766delinsCAG , CM000669.1:g.99365764_99365766delinsCAG	GRCh37
NC_000007.12:g.99203700_99203702delinsCAG	NCBI36
NG_008421.1:g.21043_21045delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.670+211_670+213delinsCTG	ENSP00000337915.3:n.670+211_670+213delinsCTG
ENST00000651514.1:c.670+211_670+213delinsCTG MANE Select	ENSP00000498939.1:n.670+211_670+213delinsCTG
ENST00000651783.1:c.211+211_211+213delinsCTG	ENSP00000498924.1:n.211+211_211+213delinsCTG
ENST00000652018.1:c.523+211_523+213delinsCTG	ENSP00000498733.1:n.523+211_523+213delinsCTG
ENST00000336411.6:c.670+211_670+213delinsCTG	ENSP00000337915.2:n.670+211_670+213delinsCTG
ENST00000354593.6:c.220+211_220+213delinsCTG	ENSP00000346607.2:n.220+211_220+213delinsCTG
NM_001202855.2:c.670+211_670+213delinsCTG	NP_001189784.1:n.670+211_670+213delinsCTG
NM_017460.5:c.670+211_670+213delinsCTG	NP_059488.2:n.670+211_670+213delinsCTG
XM_011515841.1:c.670+211_670+213delinsCTG	XP_011514143.1:n.670+211_670+213delinsCTG
XM_011515842.1:c.670+211_670+213delinsCTG	XP_011514144.1:n.670+211_670+213delinsCTG
NM_017460.6:c.670+211_670+213delinsCTG MANE Select	NP_059488.2:n.670+211_670+213delinsCTG
NM_001202855.3:c.670+211_670+213delinsCTG	NP_001189784.1:n.670+211_670+213delinsCTG