Canonical Allele Identifier: CA4369500

Gene: CYP3A4

Linked Data

• dbSNP Id: rs372741732
• ExAC: 7:99358541 G / T
• gnomAD v2: 7-99358541-G-T
• gnomAD v4: 7-99760918-G-T
• MyVariant Identifiers: chr7:g.99358541G>T (hg19) ; chr7:g.99760918G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760918G>T , CM000669.2:g.99760918G>T	GRCh38
NC_000007.13:g.99358541G>T , CM000669.1:g.99358541G>T	GRCh37
NC_000007.12:g.99196477G>T	NCBI36
NG_008421.1:g.28268C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1410C>A	ENSP00000337915.3:p.Pro470=
ENST00000651162.1:n.752C>A
ENST00000651514.1:c.1317C>A MANE Select	ENSP00000498939.1:p.Pro439=
ENST00000651783.1:c.858C>A	ENSP00000498924.1:p.Pro286=
ENST00000652018.1:c.1170C>A	ENSP00000498733.1:p.Pro390=
ENST00000336411.6:c.1317C>A	ENSP00000337915.2:p.Pro439=
ENST00000354593.6:c.867C>A	ENSP00000346607.2:p.Pro289=
NM_001202855.2:c.1314C>A	NP_001189784.1:p.Pro438=
NM_017460.5:c.1317C>A	NP_059488.2:p.Pro439=
XM_011515841.1:c.1410C>A	XP_011514143.1:p.Pro470=
XM_011515842.1:c.1407C>A	XP_011514144.1:p.Pro469=
NM_017460.6:c.1317C>A MANE Select	NP_059488.2:p.Pro439=
NM_001202855.3:c.1314C>A	NP_001189784.1:p.Pro438=