Canonical Allele Identifier: CA368367599

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358464A>G (hg19) ; chr7:g.99760841A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760841A>G , CM000669.2:g.99760841A>G	GRCh38
NC_000007.13:g.99358464A>G , CM000669.1:g.99358464A>G	GRCh37
NC_000007.12:g.99196400A>G	NCBI36
NG_008421.1:g.28345T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1487T>C	ENSP00000337915.3:p.Phe496Ser
ENST00000651162.1:n.829T>C
ENST00000651514.1:c.1394T>C MANE Select	ENSP00000498939.1:p.Phe465Ser
ENST00000651783.1:c.935T>C	ENSP00000498924.1:p.Phe312Ser
ENST00000652018.1:c.1247T>C	ENSP00000498733.1:p.Phe416Ser
ENST00000336411.6:c.1394T>C	ENSP00000337915.2:p.Phe465Ser
ENST00000354593.6:c.944T>C	ENSP00000346607.2:p.Phe315Ser
NM_001202855.2:c.1391T>C	NP_001189784.1:p.Phe464Ser
NM_017460.5:c.1394T>C	NP_059488.2:p.Phe465Ser
XM_011515841.1:c.1487T>C	XP_011514143.1:p.Phe496Ser
XM_011515842.1:c.1484T>C	XP_011514144.1:p.Phe495Ser
NM_017460.6:c.1394T>C MANE Select	NP_059488.2:p.Phe465Ser
NM_001202855.3:c.1391T>C	NP_001189784.1:p.Phe464Ser