Canonical Allele Identifier: CA368367539

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358451T>A (hg19) ; chr7:g.99760828T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760828T>A , CM000669.2:g.99760828T>A	GRCh38
NC_000007.13:g.99358451T>A , CM000669.1:g.99358451T>A	GRCh37
NC_000007.12:g.99196387T>A	NCBI36
NG_008421.1:g.28358A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.1500A>T	ENSP00000337915.3:p.Lys500Asn
ENST00000651162.1:n.842A>T
ENST00000651514.1:c.1407A>T MANE Select	ENSP00000498939.1:p.Lys469Asn
ENST00000651783.1:c.948A>T	ENSP00000498924.1:p.Lys316Asn
ENST00000652018.1:c.1260A>T	ENSP00000498733.1:p.Lys420Asn
ENST00000336411.6:c.1407A>T	ENSP00000337915.2:p.Lys469Asn
ENST00000354593.6:c.957A>T	ENSP00000346607.2:p.Lys319Asn
NM_001202855.2:c.1404A>T	NP_001189784.1:p.Lys468Asn
NM_017460.5:c.1407A>T	NP_059488.2:p.Lys469Asn
XM_011515841.1:c.1500A>T	XP_011514143.1:p.Lys500Asn
XM_011515842.1:c.1497A>T	XP_011514144.1:p.Lys499Asn
NM_017460.6:c.1407A>T MANE Select	NP_059488.2:p.Lys469Asn
NM_001202855.3:c.1404A>T	NP_001189784.1:p.Lys468Asn