Canonical Allele Identifier: CA1729176642

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1815293804

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760593_99760594insCT , CM000669.2:g.99760593_99760594insCT	GRCh38
NC_000007.13:g.99358216_99358217insCT , CM000669.1:g.99358216_99358217insCT	GRCh37
NC_000007.12:g.99196152_99196153insCT	NCBI36
NG_008421.1:g.28593_28594insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1509+226_1509+227insGA	ENSP00000337915.3:n.1509+226_1509+227insGA
ENST00000651162.1:n.851+226_851+227insGA
ENST00000651514.1:c.1416+226_1416+227insGA MANE Select	ENSP00000498939.1:n.1416+226_1416+227insGA
ENST00000651783.1:c.957+226_957+227insGA	ENSP00000498924.1:n.957+226_957+227insGA
ENST00000652018.1:c.1269+226_1269+227insGA	ENSP00000498733.1:n.1269+226_1269+227insGA
ENST00000336411.6:c.1416+226_1416+227insGA	ENSP00000337915.2:n.1416+226_1416+227insGA
ENST00000354593.6:c.966+226_966+227insGA	ENSP00000346607.2:n.966+226_966+227insGA
NM_001202855.2:c.1413+226_1413+227insGA	NP_001189784.1:n.1413+226_1413+227insGA
NM_017460.5:c.1416+226_1416+227insGA	NP_059488.2:n.1416+226_1416+227insGA
XM_011515841.1:c.1509+226_1509+227insGA	XP_011514143.1:n.1509+226_1509+227insGA
XM_011515842.1:c.1506+226_1506+227insGA	XP_011514144.1:n.1506+226_1506+227insGA
NM_017460.6:c.1416+226_1416+227insGA MANE Select	NP_059488.2:n.1416+226_1416+227insGA
NM_001202855.3:c.1413+226_1413+227insGA	NP_001189784.1:n.1413+226_1413+227insGA