Canonical Allele Identifier: CA472415386

Gene: TRPM5

Linked Data

• gnomAD v4: 11-2411641-C-T
• MyVariant Identifiers: chr11:g.2432871C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2411641C>T , CM000673.2:g.2411641C>T	GRCh38
NC_000011.9:g.2432871C>T , CM000673.1:g.2432871C>T	GRCh37
NC_000011.8:g.2389447C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000696290.1:c.2601G>A MANE Select	ENSP00000512529.1:p.Glu867=
ENST00000155858.10:c.2601G>A	ENSP00000155858.5:p.Glu867=
ENST00000528453.1:c.2601G>A	ENSP00000436809.1:p.Glu867=
ENST00000533060.5:c.2601G>A	ENSP00000434121.1:p.Glu867=
ENST00000533881.5:c.2583G>A	ENSP00000434383.1:p.Glu861=
NM_014555.3:c.2601G>A	NP_055370.1:p.Glu867=
XM_011520035.1:c.2862G>A	XP_011518337.1:p.Glu954=
XM_017017628.1:c.2655G>A	XP_016873117.1:p.Glu885=
NM_014555.4:c.2601G>A MANE Select	NP_055370.1:p.Glu867=