Canonical Allele Identifier: CA1729180874
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99768396_99768399delinsGCTT , CM000669.2:g.99768396_99768399delinsGCTT GRCh38
NC_000007.13:g.99366019_99366022delinsGCTT , CM000669.1:g.99366019_99366022delinsGCTT GRCh37
NC_000007.12:g.99203955_99203958delinsGCTT NCBI36
NG_008421.1:g.20787_20790delinsAAGC

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.625_628delinsAAGC ENSP00000337915.3:p.Lys209=
ENST00000651514.1:c.625_628delinsAAGC MANE Select ENSP00000498939.1:p.Lys209=
ENST00000651783.1:c.166_169delinsAAGC ENSP00000498924.1:p.Lys56=
ENST00000652018.1:c.478_481delinsAAGC ENSP00000498733.1:p.Lys160=
ENST00000336411.6:c.625_628delinsAAGC ENSP00000337915.2:p.Lys209=
ENST00000354593.6:c.175_178delinsAAGC ENSP00000346607.2:p.Lys59=
NM_001202855.2:c.625_628delinsAAGC NP_001189784.1:p.Lys209=
NM_017460.5:c.625_628delinsAAGC NP_059488.2:p.Lys209=
XM_011515841.1:c.625_628delinsAAGC XP_011514143.1:p.Lys209=
XM_011515842.1:c.625_628delinsAAGC XP_011514144.1:p.Lys209=
NM_017460.6:c.625_628delinsAAGC MANE Select NP_059488.2:p.Lys209=
NM_001202855.3:c.625_628delinsAAGC NP_001189784.1:p.Lys209=