Canonical Allele Identifier: CA368368902

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99762090-G-A
• MyVariant Identifiers: chr7:g.99359713G>A (hg19) ; chr7:g.99762090G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99762090G>A , CM000669.2:g.99762090G>A	GRCh38
NC_000007.13:g.99359713G>A , CM000669.1:g.99359713G>A	GRCh37
NC_000007.12:g.99197649G>A	NCBI36
NG_008421.1:g.27096C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.1204C>T	ENSP00000337915.3:p.His402Tyr
ENST00000651162.1:n.639C>T
ENST00000651514.1:c.1204C>T MANE Select	ENSP00000498939.1:p.His402Tyr
ENST00000651783.1:c.745C>T	ENSP00000498924.1:p.His249Tyr
ENST00000652018.1:c.1057C>T	ENSP00000498733.1:p.His353Tyr
ENST00000336411.6:c.1204C>T	ENSP00000337915.2:p.His402Tyr
ENST00000354593.6:c.754C>T	ENSP00000346607.2:p.His252Tyr
NM_001202855.2:c.1201C>T	NP_001189784.1:p.His401Tyr
NM_017460.5:c.1204C>T	NP_059488.2:p.His402Tyr
XM_011515841.1:c.1204C>T	XP_011514143.1:p.His402Tyr
XM_011515842.1:c.1201C>T	XP_011514144.1:p.His401Tyr
NM_017460.6:c.1204C>T MANE Select	NP_059488.2:p.His402Tyr
NM_001202855.3:c.1201C>T	NP_001189784.1:p.His401Tyr