Canonical Allele Identifier: CA456690134
Gene: CYP3A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.99366023C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99768400C>T , CM000669.2:g.99768400C>T GRCh38
NC_000007.13:g.99366023C>T , CM000669.1:g.99366023C>T GRCh37
NC_000007.12:g.99203959C>T NCBI36
NG_008421.1:g.20786G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.624G>A ENSP00000337915.3:p.Lys208=
ENST00000651514.1:c.624G>A MANE Select ENSP00000498939.1:p.Lys208=
ENST00000651783.1:c.165G>A ENSP00000498924.1:p.Lys55=
ENST00000652018.1:c.477G>A ENSP00000498733.1:p.Lys159=
ENST00000336411.6:c.624G>A ENSP00000337915.2:p.Lys208=
ENST00000354593.6:c.174G>A ENSP00000346607.2:p.Lys58=
NM_001202855.2:c.624G>A NP_001189784.1:p.Lys208=
NM_017460.5:c.624G>A NP_059488.2:p.Lys208=
XM_011515841.1:c.624G>A XP_011514143.1:p.Lys208=
XM_011515842.1:c.624G>A XP_011514144.1:p.Lys208=
NM_017460.6:c.624G>A MANE Select NP_059488.2:p.Lys208=
NM_001202855.3:c.624G>A NP_001189784.1:p.Lys208=