Canonical Allele Identifier: CA5821006
Gene: TRPM5 HGNC NCBI

Linked Data

dbSNP Id: rs143353076
gnomAD v2: 11-2432864-C-T
gnomAD v3: 11-2411634-C-T
gnomAD v4: 11-2411634-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2411634C>T , CM000673.2:g.2411634C>T GRCh38
NC_000011.9:g.2432864C>T , CM000673.1:g.2432864C>T GRCh37
NC_000011.8:g.2389440C>T NCBI36

Transcript Alleles

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