Canonical Allele Identifier: CA4520234
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs782227564
ExAC: 7:141673199 CATG / C
gnomAD v2: 7-141673199-CATG-C
gnomAD v3: 7-141973399-CATG-C
gnomAD v4: 7-141973399-CATG-C
MyVariant Identifiers: chr7:g.141673200_141673202del (hg19) chr7:g.141973400_141973402del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973406_141973408del , CM000669.2:g.141973406_141973408del GRCh38
NC_000007.13:g.141673206_141673208del , CM000669.1:g.141673206_141673208del GRCh37
NC_000007.12:g.141319675_141319677del NCBI36
NG_016141.1:g.5372_5374del

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27409_-3+27411del (MGAM) ENSP00000419372.1:n.-3+27409_-3+27411del
ENST00000547270.1:c.288_290del (TAS2R38) MANE Select ENSP00000448219.1:p.Ile96del
NM_176817.4:c.288_290del (TAS2R38) NP_789787.4:p.Ile96del
XM_011515783.1:c.*25-12990_*25-12988del (OR9A4) XP_011514085.1:n.*25-12990_*25-12988del
NM_176817.5:c.288_290del (TAS2R38) MANE Select NP_789787.5:p.Ile96del
Search 100 bp 5'
Search 100 bp 3'