Canonical Allele Identifier: CA368368639

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1457998170
• gnomAD v2: 7-99358543-G-A
• MyVariant Identifiers: chr7:g.99358543G>A (hg19) ; chr7:g.99760920G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760920G>A , CM000669.2:g.99760920G>A	GRCh38
NC_000007.13:g.99358543G>A , CM000669.1:g.99358543G>A	GRCh37
NC_000007.12:g.99196479G>A	NCBI36
NG_008421.1:g.28266C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1408C>T	ENSP00000337915.3:p.Pro470Ser
ENST00000651162.1:n.750C>T
ENST00000651514.1:c.1315C>T MANE Select	ENSP00000498939.1:p.Pro439Ser
ENST00000651783.1:c.856C>T	ENSP00000498924.1:p.Pro286Ser
ENST00000652018.1:c.1168C>T	ENSP00000498733.1:p.Pro390Ser
ENST00000336411.6:c.1315C>T	ENSP00000337915.2:p.Pro439Ser
ENST00000354593.6:c.865C>T	ENSP00000346607.2:p.Pro289Ser
NM_001202855.2:c.1312C>T	NP_001189784.1:p.Pro438Ser
NM_017460.5:c.1315C>T	NP_059488.2:p.Pro439Ser
XM_011515841.1:c.1408C>T	XP_011514143.1:p.Pro470Ser
XM_011515842.1:c.1405C>T	XP_011514144.1:p.Pro469Ser
NM_017460.6:c.1315C>T MANE Select	NP_059488.2:p.Pro439Ser
NM_001202855.3:c.1312C>T	NP_001189784.1:p.Pro438Ser