Canonical Allele Identifier: CA1748244602

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973037_141973041delinsACAGT , CM000669.2:g.141973037_141973041delinsACAGT GRCh38
NC_000007.13:g.141672837_141672841delinsACAGT , CM000669.1:g.141672837_141672841delinsACAGT GRCh37
NC_000007.12:g.141319306_141319310delinsACAGT NCBI36
NG_016141.1:g.5733_5737delinsACTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27040_-3+27044delinsACAGT (MGAM) ENSP00000419372.1:n.-3+27040_-3+27044delinsACAGT
ENST00000547270.1:c.649_653delinsACTGT (TAS2R38) MANE Select ENSP00000448219.1:p.Thr217=
NM_176817.4:c.649_653delinsACTGT (TAS2R38) NP_789787.4:p.Thr217=
XM_011515783.1:c.*25-13359_*25-13355delinsACAGT (OR9A4) XP_011514085.1:n.*25-13359_*25-13355delinsACAGT
NM_176817.5:c.649_653delinsACTGT (TAS2R38) MANE Select NP_789787.5:p.Thr217=