Canonical Allele Identifier: CA2685283448

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973370del , CM000669.2:g.141973370del GRCh38
NC_000007.13:g.141673170del , CM000669.1:g.141673170del GRCh37
NC_000007.12:g.141319639del NCBI36
NG_016141.1:g.5404del

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-3+27373del (MGAM) ENSP00000419372.1:n.-3+27373del
ENST00000547270.1:c.320del (TAS2R38) MANE Select ENSP00000448219.1:p.Leu107ProfsTer23
NM_176817.4:c.320del (TAS2R38) NP_789787.4:p.Leu107ProfsTer23
XM_011515783.1:c.*25-13026del (OR9A4) XP_011514085.1:n.*25-13026del
NM_176817.5:c.320del (TAS2R38) MANE Select NP_789787.5:p.Leu107ProfsTer23