Canonical Allele Identifier: CA1729180169

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767394C= , CM000669.2:g.99767394C=	GRCh38
NC_000007.13:g.99365017C= , CM000669.1:g.99365017C=	GRCh37
NC_000007.12:g.99202953C=	NCBI36
NG_008421.1:g.21792G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.671-136G=	ENSP00000337915.3:n.671-136G=
ENST00000651162.1:n.106-136G=
ENST00000651514.1:c.671-136G= MANE Select	ENSP00000498939.1:n.671-136G=
ENST00000651783.1:c.212-136G=	ENSP00000498924.1:n.212-136G=
ENST00000652018.1:c.524-136G=	ENSP00000498733.1:n.524-136G=
ENST00000336411.6:c.671-136G=	ENSP00000337915.2:n.671-136G=
ENST00000354593.6:c.221-136G=	ENSP00000346607.2:n.221-136G=
NM_001202855.2:c.671-139G=	NP_001189784.1:n.671-139G=
NM_017460.5:c.671-136G=	NP_059488.2:n.671-136G=
XM_011515841.1:c.671-136G=	XP_011514143.1:n.671-136G=
XM_011515842.1:c.671-139G=	XP_011514144.1:n.671-139G=
NM_017460.6:c.671-136G= MANE Select	NP_059488.2:n.671-136G=
NM_001202855.3:c.671-139G=	NP_001189784.1:n.671-139G=