Canonical Allele Identifier: CA2685283453

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973638dup , CM000669.2:g.141973638dup GRCh38
NC_000007.13:g.141673438dup , CM000669.1:g.141673438dup GRCh37
NC_000007.12:g.141319907dup NCBI36
NG_016141.1:g.5138dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000465654.5:c.-3+27641dup (MGAM) ENSP00000419372.1:n.-3+27641dup
ENST00000547270.1:c.54dup (TAS2R38) MANE Select ENSP00000448219.1:p.Leu19SerfsTer?
NM_176817.4:c.54dup (TAS2R38) NP_789787.4:p.Leu19SerfsTer?
XM_011515783.1:c.*25-12758dup (OR9A4) XP_011514085.1:n.*25-12758dup
NM_176817.5:c.54dup (TAS2R38) MANE Select NP_789787.5:p.Leu19SerfsTer?