Canonical Allele Identifier: CA1748245241

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973526_141973527delinsCA , CM000669.2:g.141973526_141973527delinsCA GRCh38
NC_000007.13:g.141673326_141673327delinsCA , CM000669.1:g.141673326_141673327delinsCA GRCh37
NC_000007.12:g.141319795_141319796delinsCA NCBI36
NG_016141.1:g.5247_5248delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27529_-3+27530delinsCA (MGAM) ENSP00000419372.1:n.-3+27529_-3+27530delinsCA
ENST00000547270.1:c.163_164delinsTG (TAS2R38) MANE Select ENSP00000448219.1:p.Cys55=
NM_176817.4:c.163_164delinsTG (TAS2R38) NP_789787.4:p.Cys55=
XM_011515783.1:c.*25-12870_*25-12869delinsCA (OR9A4) XP_011514085.1:n.*25-12870_*25-12869delinsCA
NM_176817.5:c.163_164delinsTG (TAS2R38) MANE Select NP_789787.5:p.Cys55=