Canonical Allele Identifier: CA472037925

Gene: TRPM5

Linked Data

• gnomAD v4: 11-2422935-C-T
• COSMIC: COSM3446408
• MyVariant Identifiers: chr11:g.2444165C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2422935C>T , CM000673.2:g.2422935C>T	GRCh38
NC_000011.9:g.2444165C>T , CM000673.1:g.2444165C>T	GRCh37
NC_000011.8:g.2400741C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696290.1:c.102G>A MANE Select	ENSP00000512529.1:p.Gly34=
ENST00000155858.10:c.102G>A	ENSP00000155858.5:p.Gly34=
ENST00000528453.1:c.102G>A	ENSP00000436809.1:p.Gly34=
ENST00000533060.5:c.102G>A	ENSP00000434121.1:p.Gly34=
ENST00000533881.5:c.78G>A	ENSP00000434383.1:p.Gly26=
NM_014555.3:c.102G>A	NP_055370.1:p.Gly34=
XM_011520035.1:c.363G>A	XP_011518337.1:p.Gly121=
XM_017017628.1:c.156G>A	XP_016873117.1:p.Gly52=
NM_014555.4:c.102G>A MANE Select	NP_055370.1:p.Gly34=