Canonical Allele Identifier: CA1948131369
Gene: TRPM5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2411590A= , CM000673.2:g.2411590A= GRCh38
NC_000011.9:g.2432820A= , CM000673.1:g.2432820A= GRCh37
NC_000011.8:g.2389396A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696290.1:c.2607+45T= MANE Select ENSP00000512529.1:n.2607+45T=
ENST00000155858.10:c.2607+45T= ENSP00000155858.5:n.2607+45T=
ENST00000528453.1:c.2607+45T= ENSP00000436809.1:n.2607+45T=
ENST00000533060.5:c.2607+45T= ENSP00000434121.1:n.2607+45T=
ENST00000533881.5:c.2589+45T= ENSP00000434383.1:n.2589+45T=
NM_014555.3:c.2607+45T= NP_055370.1:n.2607+45T=
XM_011520035.1:c.2868+45T= XP_011518337.1:n.2868+45T=
XM_017017628.1:c.2661+45T= XP_016873117.1:n.2661+45T=
NM_014555.4:c.2607+45T= MANE Select NP_055370.1:n.2607+45T=