Canonical Allele Identifier: CA472415402
Gene: TRPM5 HGNC NCBI

Linked Data

gnomAD v4: 11-2411665-C-T
MyVariant Identifiers: chr11:g.2432895C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2411665C>T , CM000673.2:g.2411665C>T GRCh38
NC_000011.9:g.2432895C>T , CM000673.1:g.2432895C>T GRCh37
NC_000011.8:g.2389471C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696290.1:c.2577G>A MANE Select ENSP00000512529.1:p.Leu859=
ENST00000155858.10:c.2577G>A ENSP00000155858.5:p.Leu859=
ENST00000528453.1:c.2577G>A ENSP00000436809.1:p.Leu859=
ENST00000533060.5:c.2577G>A ENSP00000434121.1:p.Leu859=
ENST00000533881.5:c.2559G>A ENSP00000434383.1:p.Leu853=
NM_014555.3:c.2577G>A NP_055370.1:p.Leu859=
XM_011520035.1:c.2838G>A XP_011518337.1:p.Leu946=
XM_017017628.1:c.2631G>A XP_016873117.1:p.Leu877=
NM_014555.4:c.2577G>A MANE Select NP_055370.1:p.Leu859=
Search 100 bp 5'
Search 100 bp 3'