Canonical Allele Identifier: CA1748244481
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs1803393268
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972943_141972944del , CM000669.2:g.141972943_141972944del GRCh38
NC_000007.13:g.141672743_141672744del , CM000669.1:g.141672743_141672744del GRCh37
NC_000007.12:g.141319212_141319213del NCBI36
NG_016141.1:g.5830_5831del

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+26946_-3+26947del (MGAM) ENSP00000419372.1:n.-3+26946_-3+26947del
ENST00000547270.1:c.746_747del (TAS2R38) MANE Select ENSP00000448219.1:p.Leu249ArgfsTer?
NM_176817.4:c.746_747del (TAS2R38) NP_789787.4:p.Leu249ArgfsTer?
XM_011515783.1:c.*25-13453_*25-13452del (OR9A4) XP_011514085.1:n.*25-13453_*25-13452del
NM_176817.5:c.746_747del (TAS2R38) MANE Select NP_789787.5:p.Leu249ArgfsTer?
Search 100 bp 5'
Search 100 bp 3'