Canonical Allele Identifier: CA472415389
Gene: TRPM5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.2432874T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2411644T>C , CM000673.2:g.2411644T>C GRCh38
NC_000011.9:g.2432874T>C , CM000673.1:g.2432874T>C GRCh37
NC_000011.8:g.2389450T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696290.1:c.2598A>G MANE Select ENSP00000512529.1:p.Val866=
ENST00000155858.10:c.2598A>G ENSP00000155858.5:p.Val866=
ENST00000528453.1:c.2598A>G ENSP00000436809.1:p.Val866=
ENST00000533060.5:c.2598A>G ENSP00000434121.1:p.Val866=
ENST00000533881.5:c.2580A>G ENSP00000434383.1:p.Val860=
NM_014555.3:c.2598A>G NP_055370.1:p.Val866=
XM_011520035.1:c.2859A>G XP_011518337.1:p.Val953=
XM_017017628.1:c.2652A>G XP_016873117.1:p.Val884=
NM_014555.4:c.2598A>G MANE Select NP_055370.1:p.Val866=
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