Canonical Allele Identifier: CA349329
Gene: TRPM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49168723G>A , CM000681.2:g.49168723G>A GRCh38
NC_000019.9:g.49671980G>A , CM000681.1:g.49671980G>A GRCh37
NC_000019.8:g.54363792G>A NCBI36
NG_027551.1:g.15965G>A
NG_027551.2:g.15965G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252826.10:c.783G>A MANE Select ENSP00000252826.4:p.Lys261=
ENST00000252826.9:c.783G>A ENSP00000252826.4:p.Lys261=
ENST00000427978.6:c.783G>A ENSP00000407492.1:p.Lys261=
ENST00000595519.5:c.*193G>A ENSP00000469893.1:n.*193G>A
ENST00000596338.5:n.818G>A
ENST00000598502.5:c.602G>A ENSP00000470229.1:p.Arg201Lys
ENST00000598691.5:c.438G>A ENSP00000473231.1:p.Lys146=
ENST00000598697.5:c.263G>A ENSP00000468989.1:p.Arg88Lys
ENST00000601347.1:n.97G>A
NM_001195227.1:c.783G>A NP_001182156.1:p.Lys261=
NM_017636.3:c.783G>A NP_060106.2:p.Lys261=
XM_005259017.1:c.-392G>A XP_005259074.1:n.-392G>A
XM_011527046.1:c.261G>A XP_011525348.1:p.Lys87=
NM_001321281.1:c.438G>A NP_001308210.1:p.Lys146=
NM_001321282.1:c.-771G>A NP_001308211.1:n.-771G>A
NM_001321283.1:c.261G>A NP_001308212.1:p.Lys87=
NM_001321285.1:c.-67G>A NP_001308214.1:n.-67G>A
XM_024451557.1:c.-1312G>A XP_024307325.1:n.-1312G>A
NM_017636.4:c.783G>A MANE Select NP_060106.2:p.Lys261=
NM_001195227.2:c.783G>A NP_001182156.1:p.Lys261=
NM_001321281.2:c.438G>A NP_001308210.1:p.Lys146=
NM_001321282.2:c.-771G>A NP_001308211.1:n.-771G>A
NM_001321283.2:c.261G>A NP_001308212.1:p.Lys87=
NM_001321285.2:c.-67G>A NP_001308214.1:n.-67G>A