Canonical Allele Identifier: CA2967067964

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973386_141973387insCATCATCATGCTATGGATGATTGCAAACCAAGCCAGAGGTTGGCTTGGTTTGC , CM000669.2:g.141973386_141973387insCATCATCATGCTATGGATGATTGCAAACCAAGCCAGAGGTTGGCTTGGTTTGC GRCh38
NC_000007.13:g.141673186_141673187insCATCATCATGCTATGGATGATTGCAAACCAAGCCAGAGGTTGGCTTGGTTTGC , CM000669.1:g.141673186_141673187insCATCATCATGCTATGGATGATTGCAAACCAAGCCAGAGGTTGGCTTGGTTTGC GRCh37
NC_000007.12:g.141319655_141319656insCATCATCATGCTATGGATGATTGCAAACCAAGCCAGAGGTTGGCTTGGTTTGC NCBI36
NG_016141.1:g.5412_5413insGTTTGCAATCATCCATAGCATGATGATGGCAAACCAAGCCAACCTCTGGCTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27389_-3+27390insCATCATCATGCTATGGATGATTGCAAACCAAGCCAGAGGTTGGCTTGGTTTGC (MGAM) ENSP00000419372.1:n.-3+27389_-3+27390insCATCATCATGCTATGGATGAT...
ENST00000547270.1:c.328_329insGTTTGCAATCATCCATAGCATGATGATGGCAAACCAAGCCAACCTCTGGCTTG (TAS2R38) MANE Select ENSP00000448219.1:p.Ala110GlyfsTer8
NM_176817.4:c.328_329insGTTTGCAATCATCCATAGCATGATGATGGCAAACCAAGCCAACCTCTGGCTTG (TAS2R38) NP_789787.4:p.Ala110GlyfsTer8
XM_011515783.1:c.*25-13010_*25-13009insCATCATCATGCTATGGATGATTGCAAACCAAGCCAGAGGTTGGCTTGGTTTGC (OR9A4) XP_011514085.1:n.*25-13010_*25-13009insCATCATCATGCTATGGATGATT...
NM_176817.5:c.328_329insGTTTGCAATCATCCATAGCATGATGATGGCAAACCAAGCCAACCTCTGGCTTG (TAS2R38) MANE Select NP_789787.5:p.Ala110GlyfsTer8