Canonical Allele Identifier: CA2685283439

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973068del , CM000669.2:g.141973068del GRCh38
NC_000007.13:g.141672868del , CM000669.1:g.141672868del GRCh37
NC_000007.12:g.141319337del NCBI36
NG_016141.1:g.5707del

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27071del (MGAM) ENSP00000419372.1:n.-3+27071del
ENST00000547270.1:c.623del (TAS2R38) MANE Select ENSP00000448219.1:p.Leu208CysfsTer9
NM_176817.4:c.623del (TAS2R38) NP_789787.4:p.Leu208CysfsTer9
XM_011515783.1:c.*25-13328del (OR9A4) XP_011514085.1:n.*25-13328del
NM_176817.5:c.623del (TAS2R38) MANE Select NP_789787.5:p.Leu208CysfsTer9