Canonical Allele Identifier: CA1948131463
Gene: TRPM5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2411637T= , CM000673.2:g.2411637T= GRCh38
NC_000011.9:g.2432867T= , CM000673.1:g.2432867T= GRCh37
NC_000011.8:g.2389443T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696290.1:c.2605A= MANE Select ENSP00000512529.1:p.Met869=
ENST00000155858.10:c.2605A= ENSP00000155858.5:p.Met869=
ENST00000528453.1:c.2605A= ENSP00000436809.1:p.Met869=
ENST00000533060.5:c.2605A= ENSP00000434121.1:p.Met869=
ENST00000533881.5:c.2587A= ENSP00000434383.1:p.Met863=
NM_014555.3:c.2605A= NP_055370.1:p.Met869=
XM_011520035.1:c.2866A= XP_011518337.1:p.Met956=
XM_017017628.1:c.2659A= XP_016873117.1:p.Met887=
NM_014555.4:c.2605A= MANE Select NP_055370.1:p.Met869=