Canonical Allele Identifier: CA368369492

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99359839C>G (hg19) ; chr7:g.99762216C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99762216C>G , CM000669.2:g.99762216C>G	GRCh38
NC_000007.13:g.99359839C>G , CM000669.1:g.99359839C>G	GRCh37
NC_000007.12:g.99197775C>G	NCBI36
NG_008421.1:g.26970G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.1078G>C	ENSP00000337915.3:p.Val360Leu
ENST00000651162.1:n.513G>C
ENST00000651514.1:c.1078G>C MANE Select	ENSP00000498939.1:p.Val360Leu
ENST00000651783.1:c.619G>C	ENSP00000498924.1:p.Val207Leu
ENST00000652018.1:c.931G>C	ENSP00000498733.1:p.Val311Leu
ENST00000336411.6:c.1078G>C	ENSP00000337915.2:p.Val360Leu
ENST00000354593.6:c.628G>C	ENSP00000346607.2:p.Val210Leu
NM_001202855.2:c.1075G>C	NP_001189784.1:p.Val359Leu
NM_017460.5:c.1078G>C	NP_059488.2:p.Val360Leu
XM_011515841.1:c.1078G>C	XP_011514143.1:p.Val360Leu
XM_011515842.1:c.1075G>C	XP_011514144.1:p.Val359Leu
NM_017460.6:c.1078G>C MANE Select	NP_059488.2:p.Val360Leu
NM_001202855.3:c.1075G>C	NP_001189784.1:p.Val359Leu