Canonical Allele Identifier: CA456686636

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99760933-G-A
• MyVariant Identifiers: chr7:g.99358556G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760933G>A , CM000669.2:g.99760933G>A	GRCh38
NC_000007.13:g.99358556G>A , CM000669.1:g.99358556G>A	GRCh37
NC_000007.12:g.99196492G>A	NCBI36
NG_008421.1:g.28253C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1395C>T	ENSP00000337915.3:p.Pro465=
ENST00000651162.1:n.737C>T
ENST00000651514.1:c.1302C>T MANE Select	ENSP00000498939.1:p.Pro434=
ENST00000651783.1:c.843C>T	ENSP00000498924.1:p.Pro281=
ENST00000652018.1:c.1155C>T	ENSP00000498733.1:p.Pro385=
ENST00000336411.6:c.1302C>T	ENSP00000337915.2:p.Pro434=
ENST00000354593.6:c.852C>T	ENSP00000346607.2:p.Pro284=
NM_001202855.2:c.1299C>T	NP_001189784.1:p.Pro433=
NM_017460.5:c.1302C>T	NP_059488.2:p.Pro434=
XM_011515841.1:c.1395C>T	XP_011514143.1:p.Pro465=
XM_011515842.1:c.1392C>T	XP_011514144.1:p.Pro464=
NM_017460.6:c.1302C>T MANE Select	NP_059488.2:p.Pro434=
NM_001202855.3:c.1299C>T	NP_001189784.1:p.Pro433=