Canonical Allele Identifier: CA379132589
Gene: TRPM5 HGNC NCBI

Linked Data

gnomAD v4: 11-2411727-C-G
MyVariant Identifiers: chr11:g.2432957C>G (hg19) chr11:g.2411727C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2411727C>G , CM000673.2:g.2411727C>G GRCh38
NC_000011.9:g.2432957C>G , CM000673.1:g.2432957C>G GRCh37
NC_000011.8:g.2389533C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696290.1:c.2515G>C MANE Select ENSP00000512529.1:p.Ala839Pro
ENST00000155858.10:c.2515G>C ENSP00000155858.5:p.Ala839Pro
ENST00000528453.1:c.2515G>C ENSP00000436809.1:p.Ala839Pro
ENST00000533060.5:c.2515G>C ENSP00000434121.1:p.Ala839Pro
ENST00000533881.5:c.2497G>C ENSP00000434383.1:p.Ala833Pro
NM_014555.3:c.2515G>C NP_055370.1:p.Ala839Pro
XM_011520035.1:c.2776G>C XP_011518337.1:p.Ala926Pro
XM_017017628.1:c.2569G>C XP_016873117.1:p.Ala857Pro
NM_014555.4:c.2515G>C MANE Select NP_055370.1:p.Ala839Pro
Search 100 bp 5'
Search 100 bp 3'