Canonical Allele Identifier: CA368368674
Gene: CYP3A4 HGNC NCBI

Linked Data

dbSNP Id: rs1355522141
gnomAD v2: 7-99358558-G-C
gnomAD v3: 7-99760935-G-C
gnomAD v4: 7-99760935-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99760935G>C , CM000669.2:g.99760935G>C GRCh38
NC_000007.13:g.99358558G>C , CM000669.1:g.99358558G>C GRCh37
NC_000007.12:g.99196494G>C NCBI36
NG_008421.1:g.28251C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.1393C>G ENSP00000337915.3:p.Pro465Ala
ENST00000651162.1:n.735C>G
ENST00000651514.1:c.1300C>G MANE Select ENSP00000498939.1:p.Pro434Ala
ENST00000651783.1:c.841C>G ENSP00000498924.1:p.Pro281Ala
ENST00000652018.1:c.1153C>G ENSP00000498733.1:p.Pro385Ala
ENST00000336411.6:c.1300C>G ENSP00000337915.2:p.Pro434Ala
ENST00000354593.6:c.850C>G ENSP00000346607.2:p.Pro284Ala
NM_001202855.2:c.1297C>G NP_001189784.1:p.Pro433Ala
NM_017460.5:c.1300C>G NP_059488.2:p.Pro434Ala
XM_011515841.1:c.1393C>G XP_011514143.1:p.Pro465Ala
XM_011515842.1:c.1390C>G XP_011514144.1:p.Pro464Ala
NM_017460.6:c.1300C>G MANE Select NP_059488.2:p.Pro434Ala
NM_001202855.3:c.1297C>G NP_001189784.1:p.Pro433Ala