Canonical Allele Identifier: CA1729180854

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768355_99768361delinsTATTGAG , CM000669.2:g.99768355_99768361delinsTATTGAG	GRCh38
NC_000007.13:g.99365978_99365984delinsTATTGAG , CM000669.1:g.99365978_99365984delinsTATTGAG	GRCh37
NC_000007.12:g.99203914_99203920delinsTATTGAG	NCBI36
NG_008421.1:g.20825_20831delinsCTCAATA

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.663_669delinsCTCAATA	ENSP00000337915.3:p.Leu221=
ENST00000651514.1:c.663_669delinsCTCAATA MANE Select	ENSP00000498939.1:p.Leu221=
ENST00000651783.1:c.204_210delinsCTCAATA	ENSP00000498924.1:p.Leu68=
ENST00000652018.1:c.516_522delinsCTCAATA	ENSP00000498733.1:p.Leu172=
ENST00000336411.6:c.663_669delinsCTCAATA	ENSP00000337915.2:p.Leu221=
ENST00000354593.6:c.213_219delinsCTCAATA	ENSP00000346607.2:p.Leu71=
NM_001202855.2:c.663_669delinsCTCAATA	NP_001189784.1:p.Leu221=
NM_017460.5:c.663_669delinsCTCAATA	NP_059488.2:p.Leu221=
XM_011515841.1:c.663_669delinsCTCAATA	XP_011514143.1:p.Leu221=
XM_011515842.1:c.663_669delinsCTCAATA	XP_011514144.1:p.Leu221=
NM_017460.6:c.663_669delinsCTCAATA MANE Select	NP_059488.2:p.Leu221=
NM_001202855.3:c.663_669delinsCTCAATA	NP_001189784.1:p.Leu221=