Canonical Allele Identifier: CA379132581
Gene: TRPM5 HGNC NCBI

Linked Data

dbSNP Id: rs1383746441
gnomAD v4: 11-2411723-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2411723A>G , CM000673.2:g.2411723A>G GRCh38
NC_000011.9:g.2432953A>G , CM000673.1:g.2432953A>G GRCh37
NC_000011.8:g.2389529A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696290.1:c.2519T>C MANE Select ENSP00000512529.1:p.Met840Thr
ENST00000155858.10:c.2519T>C ENSP00000155858.5:p.Met840Thr
ENST00000528453.1:c.2519T>C ENSP00000436809.1:p.Met840Thr
ENST00000533060.5:c.2519T>C ENSP00000434121.1:p.Met840Thr
ENST00000533881.5:c.2501T>C ENSP00000434383.1:p.Met834Thr
NM_014555.3:c.2519T>C NP_055370.1:p.Met840Thr
XM_011520035.1:c.2780T>C XP_011518337.1:p.Met927Thr
XM_017017628.1:c.2573T>C XP_016873117.1:p.Met858Thr
NM_014555.4:c.2519T>C MANE Select NP_055370.1:p.Met840Thr