Canonical Allele Identifier: CA458161354
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.141673001_141673002insT (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973201_141973202insT , CM000669.2:g.141973201_141973202insT GRCh38
NC_000007.13:g.141673001_141673002insT , CM000669.1:g.141673001_141673002insT GRCh37
NC_000007.12:g.141319470_141319471insT NCBI36
NG_016141.1:g.5572_5573insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27204_-3+27205insT (MGAM) ENSP00000419372.1:n.-3+27204_-3+27205insT
ENST00000547270.1:c.488_489insA (TAS2R38) MANE Select ENSP00000448219.1:p.Phe163LeufsTer2
NM_176817.4:c.488_489insA (TAS2R38) NP_789787.4:p.Phe163LeufsTer2
XM_011515783.1:c.*25-13195_*25-13194insT (OR9A4) XP_011514085.1:n.*25-13195_*25-13194insT
NM_176817.5:c.488_489insA (TAS2R38) MANE Select NP_789787.5:p.Phe163LeufsTer2
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