Canonical Allele Identifier: CA578624063

Linked Data

dbSNP Id: rs1803400495

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973274_141973275insCAATTTATTTTAT , CM000669.2:g.141973274_141973275insCAATTTATTTTAT GRCh38
NC_000007.13:g.141673074_141673075insCAATTTATTTTAT , CM000669.1:g.141673074_141673075insCAATTTATTTTAT GRCh37
NC_000007.12:g.141319543_141319544insCAATTTATTTTAT NCBI36
NG_016141.1:g.5500_5501insTAAAATAAATTGA

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-3+27277_-3+27278insCAATTTATTTTAT (MGAM) ENSP00000419372.1:n.-3+27277_-3+27278insC...
ENST00000547270.1:c.416_417insTAAAATAAATTGA (TAS2R38) MANE Select ENSP00000448219.1:p.Lys139AsnfsTer5
NM_176817.4:c.416_417insTAAAATAAATTGA (TAS2R38) NP_789787.4:p.Lys139AsnfsTer5
XM_011515783.1:c.*25-13122_*25-13121insCAATTTATTTTAT (OR9A4) XP_011514085.1:n.*25-13122_*25-13121insCA...
NM_176817.5:c.416_417insTAAAATAAATTGA (TAS2R38) MANE Select NP_789787.5:p.Lys139AsnfsTer5