Canonical Allele Identifier: CA9569645
Gene: TRPM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49200428A>C , CM000681.2:g.49200428A>C GRCh38
NC_000019.9:g.49703685A>C , CM000681.1:g.49703685A>C GRCh37
NC_000019.8:g.54395497A>C NCBI36
NG_027551.1:g.47670A>C
NG_027551.2:g.47670A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252826.10:c.2774A>C MANE Select ENSP00000252826.4:p.Lys925Thr
ENST00000252826.9:c.2774A>C ENSP00000252826.4:p.Lys925Thr
ENST00000427978.6:c.2339A>C ENSP00000407492.1:p.Lys780Thr
ENST00000595071.5:n.1738A>C
ENST00000595519.5:c.*2184A>C ENSP00000469893.1:n.*2184A>C
ENST00000596338.5:n.2871A>C
ENST00000598502.5:c.*1887A>C ENSP00000470229.1:n.*1887A>C
ENST00000598697.5:c.*1729A>C ENSP00000468989.1:n.*1729A>C
NM_001195227.1:c.2339A>C NP_001182156.1:p.Lys780Thr
NM_017636.3:c.2774A>C NP_060106.2:p.Lys925Thr
XM_005259017.1:c.1487A>C XP_005259074.1:p.Lys496Thr
XM_005259018.2:c.1166A>C XP_005259075.1:p.Lys389Thr
XM_011527046.1:c.2252A>C XP_011525348.1:p.Lys751Thr
NM_001321281.1:c.2429A>C NP_001308210.1:p.Lys810Thr
NM_001321282.1:c.1166A>C NP_001308211.1:p.Lys389Thr
NM_001321283.1:c.2252A>C NP_001308212.1:p.Lys751Thr
NM_001321285.1:c.1712A>C NP_001308214.1:p.Lys571Thr
XM_024451557.1:c.800A>C XP_024307325.1:p.Lys267Thr
NM_017636.4:c.2774A>C MANE Select NP_060106.2:p.Lys925Thr
NM_001195227.2:c.2339A>C NP_001182156.1:p.Lys780Thr
NM_001321281.2:c.2429A>C NP_001308210.1:p.Lys810Thr
NM_001321282.2:c.1166A>C NP_001308211.1:p.Lys389Thr
NM_001321283.2:c.2252A>C NP_001308212.1:p.Lys751Thr
NM_001321285.2:c.1712A>C NP_001308214.1:p.Lys571Thr