Canonical Allele Identifier: CA368368669

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358557G>A (hg19) ; chr7:g.99760934G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760934G>A , CM000669.2:g.99760934G>A	GRCh38
NC_000007.13:g.99358557G>A , CM000669.1:g.99358557G>A	GRCh37
NC_000007.12:g.99196493G>A	NCBI36
NG_008421.1:g.28252C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1394C>T	ENSP00000337915.3:p.Pro465Leu
ENST00000651162.1:n.736C>T
ENST00000651514.1:c.1301C>T MANE Select	ENSP00000498939.1:p.Pro434Leu
ENST00000651783.1:c.842C>T	ENSP00000498924.1:p.Pro281Leu
ENST00000652018.1:c.1154C>T	ENSP00000498733.1:p.Pro385Leu
ENST00000336411.6:c.1301C>T	ENSP00000337915.2:p.Pro434Leu
ENST00000354593.6:c.851C>T	ENSP00000346607.2:p.Pro284Leu
NM_001202855.2:c.1298C>T	NP_001189784.1:p.Pro433Leu
NM_017460.5:c.1301C>T	NP_059488.2:p.Pro434Leu
XM_011515841.1:c.1394C>T	XP_011514143.1:p.Pro465Leu
XM_011515842.1:c.1391C>T	XP_011514144.1:p.Pro464Leu
NM_017460.6:c.1301C>T MANE Select	NP_059488.2:p.Pro434Leu
NM_001202855.3:c.1298C>T	NP_001189784.1:p.Pro433Leu