Canonical Allele Identifier: CA1748245403

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973663_141973664delinsAG , CM000669.2:g.141973663_141973664delinsAG GRCh38
NC_000007.13:g.141673463_141673464delinsAG , CM000669.1:g.141673463_141673464delinsAG GRCh37
NC_000007.12:g.141319932_141319933delinsAG NCBI36
NG_016141.1:g.5110_5111delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27666_-3+27667delinsAG (MGAM) ENSP00000419372.1:n.-3+27666_-3+27667delinsAG
ENST00000547270.1:c.26_27delinsCT (TAS2R38) MANE Select ENSP00000448219.1:p.Thr9=
NM_176817.4:c.26_27delinsCT (TAS2R38) NP_789787.4:p.Thr9=
XM_011515783.1:c.*25-12733_*25-12732delinsAG (OR9A4) XP_011514085.1:n.*25-12733_*25-12732delinsAG
NM_176817.5:c.26_27delinsCT (TAS2R38) MANE Select NP_789787.5:p.Thr9=