Canonical Allele Identifier: CA578624051
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs1554444457
gnomAD v2: 7-141673460-C-CT
gnomAD v4: 7-141973660-C-CT
MyVariant Identifiers: chr7:g.141673460_141673461insT (hg19) chr7:g.141973660_141973661insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973660_141973661insT , CM000669.2:g.141973660_141973661insT GRCh38
NC_000007.13:g.141673460_141673461insT , CM000669.1:g.141673460_141673461insT GRCh37
NC_000007.12:g.141319929_141319930insT NCBI36
NG_016141.1:g.5113_5114insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27663_-3+27664insT (MGAM) ENSP00000419372.1:n.-3+27663_-3+27664insT
ENST00000547270.1:c.29_30insA (TAS2R38) MANE Select ENSP00000448219.1:p.Ser11ValfsTer3
NM_176817.4:c.29_30insA (TAS2R38) NP_789787.4:p.Ser11ValfsTer3
XM_011515783.1:c.*25-12736_*25-12735insT (OR9A4) XP_011514085.1:n.*25-12736_*25-12735insT
NM_176817.5:c.29_30insA (TAS2R38) MANE Select NP_789787.5:p.Ser11ValfsTer3
Search 100 bp 5'
Search 100 bp 3'