Canonical Allele Identifier: CA368367528

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358448T>G (hg19) ; chr7:g.99760825T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760825T>G , CM000669.2:g.99760825T>G	GRCh38
NC_000007.13:g.99358448T>G , CM000669.1:g.99358448T>G	GRCh37
NC_000007.12:g.99196384T>G	NCBI36
NG_008421.1:g.28361A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.1503A>C	ENSP00000337915.3:p.Glu501Asp
ENST00000651162.1:n.845A>C
ENST00000651514.1:c.1410A>C MANE Select	ENSP00000498939.1:p.Glu470Asp
ENST00000651783.1:c.951A>C	ENSP00000498924.1:p.Glu317Asp
ENST00000652018.1:c.1263A>C	ENSP00000498733.1:p.Glu421Asp
ENST00000336411.6:c.1410A>C	ENSP00000337915.2:p.Glu470Asp
ENST00000354593.6:c.960A>C	ENSP00000346607.2:p.Glu320Asp
NM_001202855.2:c.1407A>C	NP_001189784.1:p.Glu469Asp
NM_017460.5:c.1410A>C	NP_059488.2:p.Glu470Asp
XM_011515841.1:c.1503A>C	XP_011514143.1:p.Glu501Asp
XM_011515842.1:c.1500A>C	XP_011514144.1:p.Glu500Asp
NM_017460.6:c.1410A>C MANE Select	NP_059488.2:p.Glu470Asp
NM_001202855.3:c.1407A>C	NP_001189784.1:p.Glu469Asp