Canonical Allele Identifier: CA1748244959

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973311T= , CM000669.2:g.141973311T= GRCh38
NC_000007.13:g.141673111T= , CM000669.1:g.141673111T= GRCh37
NC_000007.12:g.141319580T= NCBI36
NG_016141.1:g.5463A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27314T= (MGAM) ENSP00000419372.1:n.-3+27314T=
ENST00000547270.1:c.379A= (TAS2R38) MANE Select ENSP00000448219.1:p.Thr127=
NM_176817.4:c.379A= (TAS2R38) NP_789787.4:p.Thr127=
XM_011515783.1:c.*25-13085T= (OR9A4) XP_011514085.1:n.*25-13085T=
NM_176817.5:c.379A= (TAS2R38) MANE Select NP_789787.5:p.Thr127=