Canonical Allele Identifier: CA2683985399

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99760938-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760939dup , CM000669.2:g.99760939dup	GRCh38
NC_000007.13:g.99358562dup , CM000669.1:g.99358562dup	GRCh37
NC_000007.12:g.99196498dup	NCBI36
NG_008421.1:g.28247dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1389dup	ENSP00000337915.3:p.Thr464HisfsTer?
ENST00000651162.1:n.731dup
ENST00000651514.1:c.1296dup MANE Select	ENSP00000498939.1:p.Thr433HisfsTer?
ENST00000651783.1:c.837dup	ENSP00000498924.1:p.Thr280HisfsTer?
ENST00000652018.1:c.1149dup	ENSP00000498733.1:p.Thr384HisfsTer?
ENST00000336411.6:c.1296dup	ENSP00000337915.2:p.Thr433HisfsTer?
ENST00000354593.6:c.846dup	ENSP00000346607.2:p.Thr283HisfsTer?
NM_001202855.2:c.1293dup	NP_001189784.1:p.Thr432HisfsTer?
NM_017460.5:c.1296dup	NP_059488.2:p.Thr433HisfsTer?
XM_011515841.1:c.1389dup	XP_011514143.1:p.Thr464HisfsTer?
XM_011515842.1:c.1386dup	XP_011514144.1:p.Thr463HisfsTer?
NM_017460.6:c.1296dup MANE Select	NP_059488.2:p.Thr433HisfsTer?
NM_001202855.3:c.1293dup	NP_001189784.1:p.Thr432HisfsTer?