Canonical Allele Identifier: CA1729181760

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1815568430

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769363_99769364insGAA , CM000669.2:g.99769363_99769364insGAA	GRCh38
NC_000007.13:g.99366986_99366987insGAA , CM000669.1:g.99366986_99366987insGAA	GRCh37
NC_000007.12:g.99204922_99204923insGAA	NCBI36
NG_008421.1:g.19823_19824insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.521+405_521+406insTCT	ENSP00000337915.3:n.521+405_521+406insTCT
ENST00000651514.1:c.521+405_521+406insTCT MANE Select	ENSP00000498939.1:n.521+405_521+406insTCT
ENST00000651783.1:c.58-856_58-855insTCT	ENSP00000498924.1:n.58-856_58-855insTCT
ENST00000652018.1:c.374+405_374+406insTCT	ENSP00000498733.1:n.374+405_374+406insTCT
ENST00000336411.6:c.521+405_521+406insTCT	ENSP00000337915.2:n.521+405_521+406insTCT
ENST00000354593.6:c.72-861_72-860insTCT	ENSP00000346607.2:n.72-861_72-860insTCT
NM_001202855.2:c.521+405_521+406insTCT	NP_001189784.1:n.521+405_521+406insTCT
NM_017460.5:c.521+405_521+406insTCT	NP_059488.2:n.521+405_521+406insTCT
XM_011515841.1:c.521+405_521+406insTCT	XP_011514143.1:n.521+405_521+406insTCT
XM_011515842.1:c.521+405_521+406insTCT	XP_011514144.1:n.521+405_521+406insTCT
NM_017460.6:c.521+405_521+406insTCT MANE Select	NP_059488.2:n.521+405_521+406insTCT
NM_001202855.3:c.521+405_521+406insTCT	NP_001189784.1:n.521+405_521+406insTCT