Canonical Allele Identifier: CA456687228

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99762217-C-T
• MyVariant Identifiers: chr7:g.99359840C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99762217C>T , CM000669.2:g.99762217C>T	GRCh38
NC_000007.13:g.99359840C>T , CM000669.1:g.99359840C>T	GRCh37
NC_000007.12:g.99197776C>T	NCBI36
NG_008421.1:g.26969G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.1077G>A	ENSP00000337915.3:p.Val359=
ENST00000651162.1:n.512G>A
ENST00000651514.1:c.1077G>A MANE Select	ENSP00000498939.1:p.Val359=
ENST00000651783.1:c.618G>A	ENSP00000498924.1:p.Val206=
ENST00000652018.1:c.930G>A	ENSP00000498733.1:p.Val310=
ENST00000336411.6:c.1077G>A	ENSP00000337915.2:p.Val359=
ENST00000354593.6:c.627G>A	ENSP00000346607.2:p.Val209=
NM_001202855.2:c.1074G>A	NP_001189784.1:p.Val358=
NM_017460.5:c.1077G>A	NP_059488.2:p.Val359=
XM_011515841.1:c.1077G>A	XP_011514143.1:p.Val359=
XM_011515842.1:c.1074G>A	XP_011514144.1:p.Val358=
NM_017460.6:c.1077G>A MANE Select	NP_059488.2:p.Val359=
NM_001202855.3:c.1074G>A	NP_001189784.1:p.Val358=