Canonical Allele Identifier: CA368368716

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358579T>A (hg19) ; chr7:g.99760956T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760956T>A , CM000669.2:g.99760956T>A	GRCh38
NC_000007.13:g.99358579T>A , CM000669.1:g.99358579T>A	GRCh37
NC_000007.12:g.99196515T>A	NCBI36
NG_008421.1:g.28230A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1372A>T	ENSP00000337915.3:p.Ile458Leu
ENST00000651162.1:n.714A>T
ENST00000651514.1:c.1279A>T MANE Select	ENSP00000498939.1:p.Ile427Leu
ENST00000651783.1:c.820A>T	ENSP00000498924.1:p.Ile274Leu
ENST00000652018.1:c.1132A>T	ENSP00000498733.1:p.Ile378Leu
ENST00000336411.6:c.1279A>T	ENSP00000337915.2:p.Ile427Leu
ENST00000354593.6:c.829A>T	ENSP00000346607.2:p.Ile277Leu
NM_001202855.2:c.1276A>T	NP_001189784.1:p.Ile426Leu
NM_017460.5:c.1279A>T	NP_059488.2:p.Ile427Leu
XM_011515841.1:c.1372A>T	XP_011514143.1:p.Ile458Leu
XM_011515842.1:c.1369A>T	XP_011514144.1:p.Ile457Leu
NM_017460.6:c.1279A>T MANE Select	NP_059488.2:p.Ile427Leu
NM_001202855.3:c.1276A>T	NP_001189784.1:p.Ile426Leu