Canonical Allele Identifier: CA9569005
Gene: TRPM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49171589C>T , CM000681.2:g.49171589C>T GRCh38
NC_000019.9:g.49674846C>T , CM000681.1:g.49674846C>T GRCh37
NC_000019.8:g.54366658C>T NCBI36
NG_027551.1:g.18831C>T
NG_027551.2:g.18831C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252826.10:c.870C>T MANE Select ENSP00000252826.4:p.Asn290=
ENST00000252826.9:c.870C>T ENSP00000252826.4:p.Asn290=
ENST00000427978.6:c.870C>T ENSP00000407492.1:p.Asn290=
ENST00000595519.5:c.*280C>T ENSP00000469893.1:n.*280C>T
ENST00000596338.5:n.905C>T
ENST00000598502.5:c.*38C>T ENSP00000470229.1:n.*38C>T
ENST00000598697.5:c.*38C>T ENSP00000468989.1:n.*38C>T
ENST00000601347.1:n.184C>T
NM_001195227.1:c.870C>T NP_001182156.1:p.Asn290=
NM_017636.3:c.870C>T NP_060106.2:p.Asn290=
XM_005259017.1:c.-305C>T XP_005259074.1:n.-305C>T
XM_011527046.1:c.348C>T XP_011525348.1:p.Asn116=
NM_001321281.1:c.525C>T NP_001308210.1:p.Asn175=
NM_001321282.1:c.-684C>T NP_001308211.1:n.-684C>T
NM_001321283.1:c.348C>T NP_001308212.1:p.Asn116=
NM_001321285.1:c.21C>T NP_001308214.1:p.Asn7=
XM_024451557.1:c.-1225C>T XP_024307325.1:n.-1225C>T
NM_017636.4:c.870C>T MANE Select NP_060106.2:p.Asn290=
NM_001195227.2:c.870C>T NP_001182156.1:p.Asn290=
NM_001321281.2:c.525C>T NP_001308210.1:p.Asn175=
NM_001321282.2:c.-684C>T NP_001308211.1:n.-684C>T
NM_001321283.2:c.348C>T NP_001308212.1:p.Asn116=
NM_001321285.2:c.21C>T NP_001308214.1:p.Asn7=