Canonical Allele Identifier: CA163151166

Gene: CYP3A4

Linked Data

• dbSNP Id: rs764639770
• gnomAD v2: 7-99358572-G-A
• gnomAD v4: 7-99760949-G-A
• MyVariant Identifiers: chr7:g.99358572G>A (hg19) ; chr7:g.99760949G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760949G>A , CM000669.2:g.99760949G>A	GRCh38
NC_000007.13:g.99358572G>A , CM000669.1:g.99358572G>A	GRCh37
NC_000007.12:g.99196508G>A	NCBI36
NG_008421.1:g.28237C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1379C>T	ENSP00000337915.3:p.Pro460Leu
ENST00000651162.1:n.721C>T
ENST00000651514.1:c.1286C>T MANE Select	ENSP00000498939.1:p.Pro429Leu
ENST00000651783.1:c.827C>T	ENSP00000498924.1:p.Pro276Leu
ENST00000652018.1:c.1139C>T	ENSP00000498733.1:p.Pro380Leu
ENST00000336411.6:c.1286C>T	ENSP00000337915.2:p.Pro429Leu
ENST00000354593.6:c.836C>T	ENSP00000346607.2:p.Pro279Leu
NM_001202855.2:c.1283C>T	NP_001189784.1:p.Pro428Leu
NM_017460.5:c.1286C>T	NP_059488.2:p.Pro429Leu
XM_011515841.1:c.1379C>T	XP_011514143.1:p.Pro460Leu
XM_011515842.1:c.1376C>T	XP_011514144.1:p.Pro459Leu
NM_017460.6:c.1286C>T MANE Select	NP_059488.2:p.Pro429Leu
NM_001202855.3:c.1283C>T	NP_001189784.1:p.Pro428Leu