Canonical Allele Identifier: CA456690198
Gene: CYP3A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.99367393T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99769770T>C , CM000669.2:g.99769770T>C GRCh38
NC_000007.13:g.99367393T>C , CM000669.1:g.99367393T>C GRCh37
NC_000007.12:g.99205329T>C NCBI36
NG_008421.1:g.19416A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.519A>G ENSP00000337915.3:p.Lys173=
ENST00000651514.1:c.519A>G MANE Select ENSP00000498939.1:p.Lys173=
ENST00000651783.1:c.58-1263A>G ENSP00000498924.1:n.58-1263A>G
ENST00000652018.1:c.372A>G ENSP00000498733.1:p.Lys124=
ENST00000336411.6:c.519A>G ENSP00000337915.2:p.Lys173=
ENST00000354593.6:c.72-1268A>G ENSP00000346607.2:n.72-1268A>G
ENST00000480043.1:n.416A>G
NM_001202855.2:c.519A>G NP_001189784.1:p.Lys173=
NM_017460.5:c.519A>G NP_059488.2:p.Lys173=
XM_011515841.1:c.519A>G XP_011514143.1:p.Lys173=
XM_011515842.1:c.519A>G XP_011514144.1:p.Lys173=
NM_017460.6:c.519A>G MANE Select NP_059488.2:p.Lys173=
NM_001202855.3:c.519A>G NP_001189784.1:p.Lys173=