Canonical Allele Identifier: CA368372812

Gene: CYP3A4

Linked Data

• dbSNP Id: rs763047916
• gnomAD v2: 7-99367407-G-C
• gnomAD v4: 7-99769784-G-C
• MyVariant Identifiers: chr7:g.99367407G>C (hg19) ; chr7:g.99769784G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769784G>C , CM000669.2:g.99769784G>C	GRCh38
NC_000007.13:g.99367407G>C , CM000669.1:g.99367407G>C	GRCh37
NC_000007.12:g.99205343G>C	NCBI36
NG_008421.1:g.19402C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.505C>G	ENSP00000337915.3:p.Pro169Ala
ENST00000651514.1:c.505C>G MANE Select	ENSP00000498939.1:p.Pro169Ala
ENST00000651783.1:c.58-1277C>G	ENSP00000498924.1:n.58-1277C>G
ENST00000652018.1:c.358C>G	ENSP00000498733.1:p.Pro120Ala
ENST00000336411.6:c.505C>G	ENSP00000337915.2:p.Pro169Ala
ENST00000354593.6:c.72-1282C>G	ENSP00000346607.2:n.72-1282C>G
ENST00000480043.1:n.402C>G
NM_001202855.2:c.505C>G	NP_001189784.1:p.Pro169Ala
NM_017460.5:c.505C>G	NP_059488.2:p.Pro169Ala
XM_011515841.1:c.505C>G	XP_011514143.1:p.Pro169Ala
XM_011515842.1:c.505C>G	XP_011514144.1:p.Pro169Ala
NM_017460.6:c.505C>G MANE Select	NP_059488.2:p.Pro169Ala
NM_001202855.3:c.505C>G	NP_001189784.1:p.Pro169Ala