Canonical Allele Identifier: CA5822019
Gene: TRPM5 HGNC NCBI

Linked Data

dbSNP Id: rs549893078
ExAC: 11:2444121 A / T
gnomAD v2: 11-2444121-A-T
gnomAD v3: 11-2422891-A-T
gnomAD v4: 11-2422891-A-T
MyVariant Identifiers: chr11:g.2444121A>T (hg19) chr11:g.2422891A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2422891A>T , CM000673.2:g.2422891A>T GRCh38
NC_000011.9:g.2444121A>T , CM000673.1:g.2444121A>T GRCh37
NC_000011.8:g.2400697A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696290.1:c.117+29T>A MANE Select ENSP00000512529.1:n.117+29T>A
ENST00000155858.10:c.117+29T>A ENSP00000155858.5:n.117+29T>A
ENST00000528453.1:c.117+29T>A ENSP00000436809.1:n.117+29T>A
ENST00000533060.5:c.117+29T>A ENSP00000434121.1:n.117+29T>A
ENST00000533881.5:c.93+29T>A ENSP00000434383.1:n.93+29T>A
NM_014555.3:c.117+29T>A NP_055370.1:n.117+29T>A
XM_011520035.1:c.378+29T>A XP_011518337.1:n.378+29T>A
XM_017017628.1:c.171+29T>A XP_016873117.1:n.171+29T>A
NM_014555.4:c.117+29T>A MANE Select NP_055370.1:n.117+29T>A
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