Canonical Allele Identifier: CA2842564528

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972727dup , CM000669.2:g.141972727dup GRCh38
NC_000007.13:g.141672527dup , CM000669.1:g.141672527dup GRCh37
NC_000007.12:g.141318996dup NCBI36
NG_016141.1:g.6048dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+26730dup (MGAM) ENSP00000419372.1:n.-3+26730dup
ENST00000547270.1:c.964dup (TAS2R38) MANE Select ENSP00000448219.1:p.Arg322LysfsTer19
NM_176817.4:c.964dup (TAS2R38) NP_789787.4:p.Arg322LysfsTer19
XM_011515783.1:c.*25-13669dup (OR9A4) XP_011514085.1:n.*25-13669dup
NM_176817.5:c.964dup (TAS2R38) MANE Select NP_789787.5:p.Arg322LysfsTer19