Canonical Allele Identifier: CA2778193693

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973218_141973219insCCCAACACA , CM000669.2:g.141973218_141973219insCCCAACACA GRCh38
NC_000007.13:g.141673018_141673019insCCCAACACA , CM000669.1:g.141673018_141673019insCCCAACACA GRCh37
NC_000007.12:g.141319487_141319488insCCCAACACA NCBI36
NG_016141.1:g.5561_5562insGGGTGTGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27221_-3+27222insCCCAACACA (MGAM) ENSP00000419372.1:n.-3+27221_-3+27222insCCCAACACA
ENST00000547270.1:c.477_478insGGGTGTGTT (TAS2R38) MANE Select ENSP00000448219.1:p.Val159_Trp160insGlyCysVal
NM_176817.4:c.477_478insGGGTGTGTT (TAS2R38) NP_789787.4:p.Val159_Trp160insGlyCysVal
XM_011515783.1:c.*25-13178_*25-13177insCCCAACACA (OR9A4) XP_011514085.1:n.*25-13178_*25-13177insCCCAACACA
NM_176817.5:c.477_478insGGGTGTGTT (TAS2R38) MANE Select NP_789787.5:p.Val159_Trp160insGlyCysVal