Canonical Allele Identifier: CA1104974997

Gene: CYP3A4

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99758352T>G , CM000669.2:g.99758352T>G	GRCh38
NC_000007.13:g.99355975T>G , CM000669.1:g.99355975T>G	GRCh37
NC_000007.12:g.99193911T>G	NCBI36
NG_008421.1:g.30834A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1510-124A>C	ENSP00000337915.3:n.1510-124A>C
ENST00000651162.1:n.852-124A>C
ENST00000651514.1:c.1417-124A>C MANE Select	ENSP00000498939.1:n.1417-124A>C
ENST00000651783.1:c.958-124A>C	ENSP00000498924.1:n.958-124A>C
ENST00000652018.1:c.1270-124A>C	ENSP00000498733.1:n.1270-124A>C
ENST00000336411.6:c.1417-124A>C	ENSP00000337915.2:n.1417-124A>C
ENST00000354593.6:c.967-124A>C	ENSP00000346607.2:n.967-124A>C
NM_001202855.2:c.1414-124A>C	NP_001189784.1:n.1414-124A>C
NM_017460.5:c.1417-124A>C	NP_059488.2:n.1417-124A>C
XM_011515841.1:c.1510-124A>C	XP_011514143.1:n.1510-124A>C
XM_011515842.1:c.1507-124A>C	XP_011514144.1:n.1507-124A>C
NM_017460.6:c.1417-124A>C MANE Select	NP_059488.2:n.1417-124A>C
NM_001202855.3:c.1414-124A>C	NP_001189784.1:n.1414-124A>C