Canonical Allele Identifier: CA934449116
Gene: TRPM5 HGNC NCBI

Linked Data

dbSNP Id: rs751393000
gnomAD v3: 11-2411601-T-A
gnomAD v4: 11-2411601-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2411601T>A , CM000673.2:g.2411601T>A GRCh38
NC_000011.9:g.2432831T>A , CM000673.1:g.2432831T>A GRCh37
NC_000011.8:g.2389407T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696290.1:c.2607+34A>T MANE Select ENSP00000512529.1:n.2607+34A>T
ENST00000155858.10:c.2607+34A>T ENSP00000155858.5:n.2607+34A>T
ENST00000528453.1:c.2607+34A>T ENSP00000436809.1:n.2607+34A>T
ENST00000533060.5:c.2607+34A>T ENSP00000434121.1:n.2607+34A>T
ENST00000533881.5:c.2589+34A>T ENSP00000434383.1:n.2589+34A>T
NM_014555.3:c.2607+34A>T NP_055370.1:n.2607+34A>T
XM_011520035.1:c.2868+34A>T XP_011518337.1:n.2868+34A>T
XM_017017628.1:c.2661+34A>T XP_016873117.1:n.2661+34A>T
NM_014555.4:c.2607+34A>T MANE Select NP_055370.1:n.2607+34A>T