Canonical Allele Identifier: CA1748245227

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973512_141973514delinsGAC , CM000669.2:g.141973512_141973514delinsGAC GRCh38
NC_000007.13:g.141673312_141673314delinsGAC , CM000669.1:g.141673312_141673314delinsGAC GRCh37
NC_000007.12:g.141319781_141319783delinsGAC NCBI36
NG_016141.1:g.5260_5262delinsGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27515_-3+27517delinsGAC (MGAM) ENSP00000419372.1:n.-3+27515_-3+27517delinsGAC
ENST00000547270.1:c.176_178delinsGTC (TAS2R38) MANE Select ENSP00000448219.1:p.Cys59=
NM_176817.4:c.176_178delinsGTC (TAS2R38) NP_789787.4:p.Cys59=
XM_011515783.1:c.*25-12884_*25-12882delinsGAC (OR9A4) XP_011514085.1:n.*25-12884_*25-12882delinsGAC
NM_176817.5:c.176_178delinsGTC (TAS2R38) MANE Select NP_789787.5:p.Cys59=