Canonical Allele Identifier: CA4369558

Gene: CYP3A4

Linked Data

• dbSNP Id: rs756833413
• ExAC: 7:99359809 C / A
• gnomAD v2: 7-99359809-C-A
• gnomAD v3: 7-99762186-C-A
• gnomAD v4: 7-99762186-C-A
• MyVariant Identifiers: chr7:g.99359809C>A (hg19) ; chr7:g.99762186C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99762186C>A , CM000669.2:g.99762186C>A	GRCh38
NC_000007.13:g.99359809C>A , CM000669.1:g.99359809C>A	GRCh37
NC_000007.12:g.99197745C>A	NCBI36
NG_008421.1:g.27000G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.1108G>T	ENSP00000337915.3:p.Ala370Ser
ENST00000651162.1:n.543G>T
ENST00000651514.1:c.1108G>T MANE Select	ENSP00000498939.1:p.Ala370Ser
ENST00000651783.1:c.649G>T	ENSP00000498924.1:p.Ala217Ser
ENST00000652018.1:c.961G>T	ENSP00000498733.1:p.Ala321Ser
ENST00000336411.6:c.1108G>T	ENSP00000337915.2:p.Ala370Ser
ENST00000354593.6:c.658G>T	ENSP00000346607.2:p.Ala220Ser
NM_001202855.2:c.1105G>T	NP_001189784.1:p.Ala369Ser
NM_017460.5:c.1108G>T	NP_059488.2:p.Ala370Ser
XM_011515841.1:c.1108G>T	XP_011514143.1:p.Ala370Ser
XM_011515842.1:c.1105G>T	XP_011514144.1:p.Ala369Ser
NM_017460.6:c.1108G>T MANE Select	NP_059488.2:p.Ala370Ser
NM_001202855.3:c.1105G>T	NP_001189784.1:p.Ala369Ser