Canonical Allele Identifier: CA4520201
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs782449246
ExAC: 7:141673045 GAAT / G
gnomAD v2: 7-141673045-GAAT-G
gnomAD v4: 7-141973245-GAAT-G
MyVariant Identifiers: chr7:g.141673046_141673048del (hg19) chr7:g.141973246_141973248del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973250_141973252del , CM000669.2:g.141973250_141973252del GRCh38
NC_000007.13:g.141673050_141673052del , CM000669.1:g.141673050_141673052del GRCh37
NC_000007.12:g.141319519_141319521del NCBI36
NG_016141.1:g.5526_5528del

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27253_-3+27255del (MGAM) ENSP00000419372.1:n.-3+27253_-3+27255del
ENST00000547270.1:c.442_444del (TAS2R38) MANE Select ENSP00000448219.1:p.Ile148del
NM_176817.4:c.442_444del (TAS2R38) NP_789787.4:p.Ile148del
XM_011515783.1:c.*25-13146_*25-13144del (OR9A4) XP_011514085.1:n.*25-13146_*25-13144del
NM_176817.5:c.442_444del (TAS2R38) MANE Select NP_789787.5:p.Ile148del
Search 100 bp 5'
Search 100 bp 3'