Canonical Allele Identifier: CA4369498

Gene: CYP3A4

Linked Data

• dbSNP Id: rs4986910
• ExAC: 7:99358524 A / G
• gnomAD v2: 7-99358524-A-G
• gnomAD v3: 7-99760901-A-G
• gnomAD v4: 7-99760901-A-G
• MyVariant Identifiers: chr7:g.99358524A>G (hg19) ; chr7:g.99760901A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760901A>G , CM000669.2:g.99760901A>G	GRCh38
NC_000007.13:g.99358524A>G , CM000669.1:g.99358524A>G	GRCh37
NC_000007.12:g.99196460A>G	NCBI36
NG_008421.1:g.28285T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1427T>C	ENSP00000337915.3:p.Met476Thr
ENST00000651162.1:n.769T>C
ENST00000651514.1:c.1334T>C MANE Select	ENSP00000498939.1:p.Met445Thr
ENST00000651783.1:c.875T>C	ENSP00000498924.1:p.Met292Thr
ENST00000652018.1:c.1187T>C	ENSP00000498733.1:p.Met396Thr
ENST00000336411.6:c.1334T>C	ENSP00000337915.2:p.Met445Thr
ENST00000354593.6:c.884T>C	ENSP00000346607.2:p.Met295Thr
NM_001202855.2:c.1331T>C	NP_001189784.1:p.Met444Thr
NM_017460.5:c.1334T>C	NP_059488.2:p.Met445Thr
XM_011515841.1:c.1427T>C	XP_011514143.1:p.Met476Thr
XM_011515842.1:c.1424T>C	XP_011514144.1:p.Met475Thr
NM_017460.6:c.1334T>C MANE Select	NP_059488.2:p.Met445Thr
NM_001202855.3:c.1331T>C	NP_001189784.1:p.Met444Thr