Canonical Allele Identifier: CA597107359

Gene: TRPM5

Linked Data

• dbSNP Id: rs1432350766
• gnomAD v2: 11-2444104-T-G
• gnomAD v4: 11-2422874-T-G
• MyVariant Identifiers: chr11:g.2444104T>G (hg19) ; chr11:g.2422874T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2422874T>G , CM000673.2:g.2422874T>G	GRCh38
NC_000011.9:g.2444104T>G , CM000673.1:g.2444104T>G	GRCh37
NC_000011.8:g.2400680T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000696290.1:c.117+46A>C MANE Select	ENSP00000512529.1:n.117+46A>C
ENST00000155858.10:c.117+46A>C	ENSP00000155858.5:n.117+46A>C
ENST00000528453.1:c.117+46A>C	ENSP00000436809.1:n.117+46A>C
ENST00000533060.5:c.117+46A>C	ENSP00000434121.1:n.117+46A>C
ENST00000533881.5:c.93+46A>C	ENSP00000434383.1:n.93+46A>C
NM_014555.3:c.117+46A>C	NP_055370.1:n.117+46A>C
XM_011520035.1:c.378+46A>C	XP_011518337.1:n.378+46A>C
XM_017017628.1:c.171+46A>C	XP_016873117.1:n.171+46A>C
NM_014555.4:c.117+46A>C MANE Select	NP_055370.1:n.117+46A>C