Canonical Allele Identifier: CA456690151

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99768427-T-C
• MyVariant Identifiers: chr7:g.99366050T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768427T>C , CM000669.2:g.99768427T>C	GRCh38
NC_000007.13:g.99366050T>C , CM000669.1:g.99366050T>C	GRCh37
NC_000007.12:g.99203986T>C	NCBI36
NG_008421.1:g.20759A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.597A>G	ENSP00000337915.3:p.Pro199=
ENST00000651514.1:c.597A>G MANE Select	ENSP00000498939.1:p.Pro199=
ENST00000651783.1:c.138A>G	ENSP00000498924.1:p.Pro46=
ENST00000652018.1:c.450A>G	ENSP00000498733.1:p.Pro150=
ENST00000336411.6:c.597A>G	ENSP00000337915.2:p.Pro199=
ENST00000354593.6:c.147A>G	ENSP00000346607.2:p.Pro49=
NM_001202855.2:c.597A>G	NP_001189784.1:p.Pro199=
NM_017460.5:c.597A>G	NP_059488.2:p.Pro199=
XM_011515841.1:c.597A>G	XP_011514143.1:p.Pro199=
XM_011515842.1:c.597A>G	XP_011514144.1:p.Pro199=
NM_017460.6:c.597A>G MANE Select	NP_059488.2:p.Pro199=
NM_001202855.3:c.597A>G	NP_001189784.1:p.Pro199=