Canonical Allele Identifier: CA2612001799
Gene: TRPM5 HGNC NCBI

Linked Data

gnomAD v4: 11-2422873-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2422873T>G , CM000673.2:g.2422873T>G GRCh38
NC_000011.9:g.2444103T>G , CM000673.1:g.2444103T>G GRCh37
NC_000011.8:g.2400679T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696290.1:c.117+47A>C MANE Select ENSP00000512529.1:n.117+47A>C
ENST00000155858.10:c.117+47A>C ENSP00000155858.5:n.117+47A>C
ENST00000528453.1:c.117+47A>C ENSP00000436809.1:n.117+47A>C
ENST00000533060.5:c.117+47A>C ENSP00000434121.1:n.117+47A>C
ENST00000533881.5:c.93+47A>C ENSP00000434383.1:n.93+47A>C
NM_014555.3:c.117+47A>C NP_055370.1:n.117+47A>C
XM_011520035.1:c.378+47A>C XP_011518337.1:n.378+47A>C
XM_017017628.1:c.171+47A>C XP_016873117.1:n.171+47A>C
NM_014555.4:c.117+47A>C MANE Select NP_055370.1:n.117+47A>C