Canonical Allele Identifier: CA1729179889

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767089_99767090delinsTG , CM000669.2:g.99767089_99767090delinsTG	GRCh38
NC_000007.13:g.99364712_99364713delinsTG , CM000669.1:g.99364712_99364713delinsTG	GRCh37
NC_000007.12:g.99202648_99202649delinsTG	NCBI36
NG_008421.1:g.22096_22097delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.798+41_798+42delinsCA	ENSP00000337915.3:n.798+41_798+42delinsCA
ENST00000651162.1:n.233+41_233+42delinsCA
ENST00000651514.1:c.798+41_798+42delinsCA MANE Select	ENSP00000498939.1:n.798+41_798+42delinsCA
ENST00000651783.1:c.339+41_339+42delinsCA	ENSP00000498924.1:n.339+41_339+42delinsCA
ENST00000652018.1:c.651+41_651+42delinsCA	ENSP00000498733.1:n.651+41_651+42delinsCA
ENST00000336411.6:c.798+41_798+42delinsCA	ENSP00000337915.2:n.798+41_798+42delinsCA
ENST00000354593.6:c.348+41_348+42delinsCA	ENSP00000346607.2:n.348+41_348+42delinsCA
NM_001202855.2:c.795+41_795+42delinsCA	NP_001189784.1:n.795+41_795+42delinsCA
NM_017460.5:c.798+41_798+42delinsCA	NP_059488.2:n.798+41_798+42delinsCA
XM_011515841.1:c.798+41_798+42delinsCA	XP_011514143.1:n.798+41_798+42delinsCA
XM_011515842.1:c.795+41_795+42delinsCA	XP_011514144.1:n.795+41_795+42delinsCA
NM_017460.6:c.798+41_798+42delinsCA MANE Select	NP_059488.2:n.798+41_798+42delinsCA
NM_001202855.3:c.795+41_795+42delinsCA	NP_001189784.1:n.795+41_795+42delinsCA