Canonical Allele Identifier: CA368370671

Gene: CYP3A4

Linked Data

• COSMIC: COSM3642945
• MyVariant Identifiers: chr7:g.99365994G>A (hg19) ; chr7:g.99768371G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768371G>A , CM000669.2:g.99768371G>A	GRCh38
NC_000007.13:g.99365994G>A , CM000669.1:g.99365994G>A	GRCh37
NC_000007.12:g.99203930G>A	NCBI36
NG_008421.1:g.20815C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.653C>T	ENSP00000337915.3:p.Pro218Leu
ENST00000651514.1:c.653C>T MANE Select	ENSP00000498939.1:p.Pro218Leu
ENST00000651783.1:c.194C>T	ENSP00000498924.1:p.Pro65Leu
ENST00000652018.1:c.506C>T	ENSP00000498733.1:p.Pro169Leu
ENST00000336411.6:c.653C>T	ENSP00000337915.2:p.Pro218Leu
ENST00000354593.6:c.203C>T	ENSP00000346607.2:p.Pro68Leu
NM_001202855.2:c.653C>T	NP_001189784.1:p.Pro218Leu
NM_017460.5:c.653C>T	NP_059488.2:p.Pro218Leu
XM_011515841.1:c.653C>T	XP_011514143.1:p.Pro218Leu
XM_011515842.1:c.653C>T	XP_011514144.1:p.Pro218Leu
NM_017460.6:c.653C>T MANE Select	NP_059488.2:p.Pro218Leu
NM_001202855.3:c.653C>T	NP_001189784.1:p.Pro218Leu