Canonical Allele Identifier: CA4520121

Linked Data

dbSNP Id: rs781915615

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141972728dup , CM000669.2:g.141972728dup GRCh38
NC_000007.13:g.141672528dup , CM000669.1:g.141672528dup GRCh37
NC_000007.12:g.141318997dup NCBI36
NG_016141.1:g.6046dup

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-3+26731dup (MGAM) ENSP00000419372.1:n.-3+26731dup
ENST00000547270.1:c.962dup (TAS2R38) MANE Select ENSP00000448219.1:p.Arg322LysfsTer19
NM_176817.4:c.962dup (TAS2R38) NP_789787.4:p.Arg322LysfsTer19
XM_011515783.1:c.*25-13668dup (OR9A4) XP_011514085.1:n.*25-13668dup
NM_176817.5:c.962dup (TAS2R38) MANE Select NP_789787.5:p.Arg322LysfsTer19