Canonical Allele Identifier: CA472415398
Gene: TRPM5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.2432889G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2411659G>A , CM000673.2:g.2411659G>A GRCh38
NC_000011.9:g.2432889G>A , CM000673.1:g.2432889G>A GRCh37
NC_000011.8:g.2389465G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696290.1:c.2583C>T MANE Select ENSP00000512529.1:p.Pro861=
ENST00000155858.10:c.2583C>T ENSP00000155858.5:p.Pro861=
ENST00000528453.1:c.2583C>T ENSP00000436809.1:p.Pro861=
ENST00000533060.5:c.2583C>T ENSP00000434121.1:p.Pro861=
ENST00000533881.5:c.2565C>T ENSP00000434383.1:p.Pro855=
NM_014555.3:c.2583C>T NP_055370.1:p.Pro861=
XM_011520035.1:c.2844C>T XP_011518337.1:p.Pro948=
XM_017017628.1:c.2637C>T XP_016873117.1:p.Pro879=
NM_014555.4:c.2583C>T MANE Select NP_055370.1:p.Pro861=