Canonical Allele Identifier: CA368367513

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358444G>T (hg19) ; chr7:g.99760821G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760821G>T , CM000669.2:g.99760821G>T	GRCh38
NC_000007.13:g.99358444G>T , CM000669.1:g.99358444G>T	GRCh37
NC_000007.12:g.99196380G>T	NCBI36
NG_008421.1:g.28365C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.1507C>A	ENSP00000337915.3:p.Gln503Lys
ENST00000651162.1:n.849C>A
ENST00000651514.1:c.1414C>A MANE Select	ENSP00000498939.1:p.Gln472Lys
ENST00000651783.1:c.955C>A	ENSP00000498924.1:p.Gln319Lys
ENST00000652018.1:c.1267C>A	ENSP00000498733.1:p.Gln423Lys
ENST00000336411.6:c.1414C>A	ENSP00000337915.2:p.Gln472Lys
ENST00000354593.6:c.964C>A	ENSP00000346607.2:p.Gln322Lys
NM_001202855.2:c.1411C>A	NP_001189784.1:p.Gln471Lys
NM_017460.5:c.1414C>A	NP_059488.2:p.Gln472Lys
XM_011515841.1:c.1507C>A	XP_011514143.1:p.Gln503Lys
XM_011515842.1:c.1504C>A	XP_011514144.1:p.Gln502Lys
NM_017460.6:c.1414C>A MANE Select	NP_059488.2:p.Gln472Lys
NM_001202855.3:c.1411C>A	NP_001189784.1:p.Gln471Lys