Canonical Allele Identifier: CA2580595029

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767460G>C , CM000669.2:g.99767460G>C	GRCh38
NC_000007.13:g.99365083G>C , CM000669.1:g.99365083G>C	GRCh37
NC_000007.12:g.99203019G>C	NCBI36
NG_008421.1:g.21726C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.671-202C>G	ENSP00000337915.3:n.671-202C>G
ENST00000651162.1:n.106-202C>G
ENST00000651514.1:c.671-202C>G MANE Select	ENSP00000498939.1:n.671-202C>G
ENST00000651783.1:c.212-202C>G	ENSP00000498924.1:n.212-202C>G
ENST00000652018.1:c.524-202C>G	ENSP00000498733.1:n.524-202C>G
ENST00000336411.6:c.671-202C>G	ENSP00000337915.2:n.671-202C>G
ENST00000354593.6:c.221-202C>G	ENSP00000346607.2:n.221-202C>G
NM_001202855.2:c.671-205C>G	NP_001189784.1:n.671-205C>G
NM_017460.5:c.671-202C>G	NP_059488.2:n.671-202C>G
XM_011515841.1:c.671-202C>G	XP_011514143.1:n.671-202C>G
XM_011515842.1:c.671-205C>G	XP_011514144.1:n.671-205C>G
NM_017460.6:c.671-202C>G MANE Select	NP_059488.2:n.671-202C>G
NM_001202855.3:c.671-205C>G	NP_001189784.1:n.671-205C>G