Canonical Allele Identifier: CA844513992
Gene: CYP3A4 HGNC NCBI

Linked Data

dbSNP Id: rs1477539005
MyVariant Identifiers: chr7:g.99365148_99365149insC (hg19) chr7:g.99767525_99767526insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99767528dup , CM000669.2:g.99767528dup GRCh38
NC_000007.13:g.99365151dup , CM000669.1:g.99365151dup GRCh37
NC_000007.12:g.99203087dup NCBI36
NG_008421.1:g.21660dup

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.671-268dup ENSP00000337915.3:n.671-268dup
ENST00000651162.1:n.105+192dup
ENST00000651514.1:c.671-268dup MANE Select ENSP00000498939.1:n.671-268dup
ENST00000651783.1:c.212-268dup ENSP00000498924.1:n.212-268dup
ENST00000652018.1:c.524-268dup ENSP00000498733.1:n.524-268dup
ENST00000336411.6:c.671-268dup ENSP00000337915.2:n.671-268dup
ENST00000354593.6:c.221-268dup ENSP00000346607.2:n.221-268dup
NM_001202855.2:c.671-271dup NP_001189784.1:n.671-271dup
NM_017460.5:c.671-268dup NP_059488.2:n.671-268dup
XM_011515841.1:c.671-268dup XP_011514143.1:n.671-268dup
XM_011515842.1:c.671-271dup XP_011514144.1:n.671-271dup
NM_017460.6:c.671-268dup MANE Select NP_059488.2:n.671-268dup
NM_001202855.3:c.671-271dup NP_001189784.1:n.671-271dup
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