Canonical Allele Identifier: CA1729181727

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1815567692

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769344dup , CM000669.2:g.99769344dup	GRCh38
NC_000007.13:g.99366967dup , CM000669.1:g.99366967dup	GRCh37
NC_000007.12:g.99204903dup	NCBI36
NG_008421.1:g.19848dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.521+430dup	ENSP00000337915.3:n.521+430dup
ENST00000651514.1:c.521+430dup MANE Select	ENSP00000498939.1:n.521+430dup
ENST00000651783.1:c.58-831dup	ENSP00000498924.1:n.58-831dup
ENST00000652018.1:c.374+430dup	ENSP00000498733.1:n.374+430dup
ENST00000336411.6:c.521+430dup	ENSP00000337915.2:n.521+430dup
ENST00000354593.6:c.72-836dup	ENSP00000346607.2:n.72-836dup
NM_001202855.2:c.521+430dup	NP_001189784.1:n.521+430dup
NM_017460.5:c.521+430dup	NP_059488.2:n.521+430dup
XM_011515841.1:c.521+430dup	XP_011514143.1:n.521+430dup
XM_011515842.1:c.521+430dup	XP_011514144.1:n.521+430dup
NM_017460.6:c.521+430dup MANE Select	NP_059488.2:n.521+430dup
NM_001202855.3:c.521+430dup	NP_001189784.1:n.521+430dup