Canonical Allele Identifier: CA472415390
Gene: TRPM5 HGNC NCBI

Linked Data

dbSNP Id: rs368193412
MyVariant Identifiers: chr11:g.2432877C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2411647C>G , CM000673.2:g.2411647C>G GRCh38
NC_000011.9:g.2432877C>G , CM000673.1:g.2432877C>G GRCh37
NC_000011.8:g.2389453C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696290.1:c.2595G>C MANE Select ENSP00000512529.1:p.Val865=
ENST00000155858.10:c.2595G>C ENSP00000155858.5:p.Val865=
ENST00000528453.1:c.2595G>C ENSP00000436809.1:p.Val865=
ENST00000533060.5:c.2595G>C ENSP00000434121.1:p.Val865=
ENST00000533881.5:c.2577G>C ENSP00000434383.1:p.Val859=
NM_014555.3:c.2595G>C NP_055370.1:p.Val865=
XM_011520035.1:c.2856G>C XP_011518337.1:p.Val952=
XM_017017628.1:c.2649G>C XP_016873117.1:p.Val883=
NM_014555.4:c.2595G>C MANE Select NP_055370.1:p.Val865=
Search 100 bp 5'
Search 100 bp 3'