Canonical Allele Identifier: CA578624050
Gene: MGAM HGNC NCBI
TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

dbSNP Id: rs1554444456
gnomAD v2: 7-141673450-CT-C
gnomAD v4: 7-141973650-CT-C
MyVariant Identifiers: chr7:g.141673451del (hg19) chr7:g.141973651del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973652del , CM000669.2:g.141973652del GRCh38
NC_000007.13:g.141673452del , CM000669.1:g.141673452del GRCh37
NC_000007.12:g.141319921del NCBI36
NG_016141.1:g.5123del

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27655del (MGAM) ENSP00000419372.1:n.-3+27655del
ENST00000547270.1:c.39del (TAS2R38) MANE Select ENSP00000448219.1:p.Val14SerfsTer18
NM_176817.4:c.39del (TAS2R38) NP_789787.4:p.Val14SerfsTer18
XM_011515783.1:c.*25-12744del (OR9A4) XP_011514085.1:n.*25-12744del
NM_176817.5:c.39del (TAS2R38) MANE Select NP_789787.5:p.Val14SerfsTer18
Search 100 bp 5'
Search 100 bp 3'