Canonical Allele Identifier: CA2685283438
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

gnomAD v4: 7-141972998-G-GT
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972999dup , CM000669.2:g.141972999dup GRCh38
NC_000007.13:g.141672799dup , CM000669.1:g.141672799dup GRCh37
NC_000007.12:g.141319268dup NCBI36
NG_016141.1:g.5775dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27002dup (MGAM) ENSP00000419372.1:n.-3+27002dup
ENST00000547270.1:c.691dup (TAS2R38) MANE Select ENSP00000448219.1:p.Thr231AsnfsTer6
NM_176817.4:c.691dup (TAS2R38) NP_789787.4:p.Thr231AsnfsTer6
XM_011515783.1:c.*25-13397dup (OR9A4) XP_011514085.1:n.*25-13397dup
NM_176817.5:c.691dup (TAS2R38) MANE Select NP_789787.5:p.Thr231AsnfsTer6
Search 100 bp 5'
Search 100 bp 3'