Canonical Allele Identifier: CA368368562

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358508C>G (hg19) ; chr7:g.99760885C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760885C>G , CM000669.2:g.99760885C>G	GRCh38
NC_000007.13:g.99358508C>G , CM000669.1:g.99358508C>G	GRCh37
NC_000007.12:g.99196444C>G	NCBI36
NG_008421.1:g.28301G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1443G>C	ENSP00000337915.3:p.Met481Ile
ENST00000651162.1:n.785G>C
ENST00000651514.1:c.1350G>C MANE Select	ENSP00000498939.1:p.Met450Ile
ENST00000651783.1:c.891G>C	ENSP00000498924.1:p.Met297Ile
ENST00000652018.1:c.1203G>C	ENSP00000498733.1:p.Met401Ile
ENST00000336411.6:c.1350G>C	ENSP00000337915.2:p.Met450Ile
ENST00000354593.6:c.900G>C	ENSP00000346607.2:p.Met300Ile
NM_001202855.2:c.1347G>C	NP_001189784.1:p.Met449Ile
NM_017460.5:c.1350G>C	NP_059488.2:p.Met450Ile
XM_011515841.1:c.1443G>C	XP_011514143.1:p.Met481Ile
XM_011515842.1:c.1440G>C	XP_011514144.1:p.Met480Ile
NM_017460.6:c.1350G>C MANE Select	NP_059488.2:p.Met450Ile
NM_001202855.3:c.1347G>C	NP_001189784.1:p.Met449Ile