Canonical Allele Identifier: CA368370220

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99364785A>G (hg19) ; chr7:g.99767162A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767162A>G , CM000669.2:g.99767162A>G	GRCh38
NC_000007.13:g.99364785A>G , CM000669.1:g.99364785A>G	GRCh37
NC_000007.12:g.99202721A>G	NCBI36
NG_008421.1:g.22024T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.767T>C	ENSP00000337915.3:p.Met256Thr
ENST00000651162.1:n.202T>C
ENST00000651514.1:c.767T>C MANE Select	ENSP00000498939.1:p.Met256Thr
ENST00000651783.1:c.308T>C	ENSP00000498924.1:p.Met103Thr
ENST00000652018.1:c.620T>C	ENSP00000498733.1:p.Met207Thr
ENST00000336411.6:c.767T>C	ENSP00000337915.2:p.Met256Thr
ENST00000354593.6:c.317T>C	ENSP00000346607.2:p.Met106Thr
NM_001202855.2:c.764T>C	NP_001189784.1:p.Met255Thr
NM_017460.5:c.767T>C	NP_059488.2:p.Met256Thr
XM_011515841.1:c.767T>C	XP_011514143.1:p.Met256Thr
XM_011515842.1:c.764T>C	XP_011514144.1:p.Met255Thr
NM_017460.6:c.767T>C MANE Select	NP_059488.2:p.Met256Thr
NM_001202855.3:c.764T>C	NP_001189784.1:p.Met255Thr