Canonical Allele Identifier: CA379132549
Gene: TRPM5 HGNC NCBI

Linked Data

dbSNP Id: rs1850455629

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2411711A>G , CM000673.2:g.2411711A>G GRCh38
NC_000011.9:g.2432941A>G , CM000673.1:g.2432941A>G GRCh37
NC_000011.8:g.2389517A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696290.1:c.2531T>C MANE Select ENSP00000512529.1:p.Val844Ala
ENST00000155858.10:c.2531T>C ENSP00000155858.5:p.Val844Ala
ENST00000528453.1:c.2531T>C ENSP00000436809.1:p.Val844Ala
ENST00000533060.5:c.2531T>C ENSP00000434121.1:p.Val844Ala
ENST00000533881.5:c.2513T>C ENSP00000434383.1:p.Val838Ala
NM_014555.3:c.2531T>C NP_055370.1:p.Val844Ala
XM_011520035.1:c.2792T>C XP_011518337.1:p.Val931Ala
XM_017017628.1:c.2585T>C XP_016873117.1:p.Val862Ala
NM_014555.4:c.2531T>C MANE Select NP_055370.1:p.Val844Ala