Canonical Allele Identifier: CA368368614

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358532G>C (hg19) ; chr7:g.99760909G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760909G>C , CM000669.2:g.99760909G>C	GRCh38
NC_000007.13:g.99358532G>C , CM000669.1:g.99358532G>C	GRCh37
NC_000007.12:g.99196468G>C	NCBI36
NG_008421.1:g.28277C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1419C>G	ENSP00000337915.3:p.Cys473Trp
ENST00000651162.1:n.761C>G
ENST00000651514.1:c.1326C>G MANE Select	ENSP00000498939.1:p.Cys442Trp
ENST00000651783.1:c.867C>G	ENSP00000498924.1:p.Cys289Trp
ENST00000652018.1:c.1179C>G	ENSP00000498733.1:p.Cys393Trp
ENST00000336411.6:c.1326C>G	ENSP00000337915.2:p.Cys442Trp
ENST00000354593.6:c.876C>G	ENSP00000346607.2:p.Cys292Trp
NM_001202855.2:c.1323C>G	NP_001189784.1:p.Cys441Trp
NM_017460.5:c.1326C>G	NP_059488.2:p.Cys442Trp
XM_011515841.1:c.1419C>G	XP_011514143.1:p.Cys473Trp
XM_011515842.1:c.1416C>G	XP_011514144.1:p.Cys472Trp
NM_017460.6:c.1326C>G MANE Select	NP_059488.2:p.Cys442Trp
NM_001202855.3:c.1323C>G	NP_001189784.1:p.Cys441Trp