Canonical Allele Identifier: CA2685283447

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973348_141973365dup , CM000669.2:g.141973348_141973365dup GRCh38
NC_000007.13:g.141673148_141673165dup , CM000669.1:g.141673148_141673165dup GRCh37
NC_000007.12:g.141319617_141319634dup NCBI36
NG_016141.1:g.5411_5428dup

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-3+27351_-3+27368dup (MGAM) ENSP00000419372.1:n.-3+27351_-3+27368dup
ENST00000547270.1:c.327_344dup (TAS2R38) MANE Select ENSP00000448219.1:p.Leu115_Leu116insAlaAl...
NM_176817.4:c.327_344dup (TAS2R38) NP_789787.4:p.Leu115_Leu116insAlaAlaCysLe...
XM_011515783.1:c.*25-13048_*25-13031dup (OR9A4) XP_011514085.1:n.*25-13048_*25-13031dup
NM_176817.5:c.327_344dup (TAS2R38) MANE Select NP_789787.5:p.Leu115_Leu116insAlaAlaCysLe...