Canonical Allele Identifier: CA368371029

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99366056G>C (hg19) ; chr7:g.99768433G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768433G>C , CM000669.2:g.99768433G>C	GRCh38
NC_000007.13:g.99366056G>C , CM000669.1:g.99366056G>C	GRCh37
NC_000007.12:g.99203992G>C	NCBI36
NG_008421.1:g.20753C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.591C>G	ENSP00000337915.3:p.Asn197Lys
ENST00000651514.1:c.591C>G MANE Select	ENSP00000498939.1:p.Asn197Lys
ENST00000651783.1:c.132C>G	ENSP00000498924.1:p.Asn44Lys
ENST00000652018.1:c.444C>G	ENSP00000498733.1:p.Asn148Lys
ENST00000336411.6:c.591C>G	ENSP00000337915.2:p.Asn197Lys
ENST00000354593.6:c.141C>G	ENSP00000346607.2:p.Asn47Lys
NM_001202855.2:c.591C>G	NP_001189784.1:p.Asn197Lys
NM_017460.5:c.591C>G	NP_059488.2:p.Asn197Lys
XM_011515841.1:c.591C>G	XP_011514143.1:p.Asn197Lys
XM_011515842.1:c.591C>G	XP_011514144.1:p.Asn197Lys
NM_017460.6:c.591C>G MANE Select	NP_059488.2:p.Asn197Lys
NM_001202855.3:c.591C>G	NP_001189784.1:p.Asn197Lys