Canonical Allele Identifier: CA9568660
Gene: TRPM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49158271G>A , CM000681.2:g.49158271G>A GRCh38
NC_000019.9:g.49661528G>A , CM000681.1:g.49661528G>A GRCh37
NC_000019.8:g.54353340G>A NCBI36
NG_027551.1:g.5513G>A
NG_027551.2:g.5513G>A

Transcript Alleles

HGVS Amino-acid Change
NM_017636.4:c.92+12G>A MANE Select NP_060106.2:n.92+12G>A
ENST00000252826.10:c.92+12G>A MANE Select ENSP00000252826.4:n.92+12G>A
NM_001195227.1:c.92+12G>A NP_001182156.1:n.92+12G>A
NM_001195227.2:c.92+12G>A NP_001182156.1:n.92+12G>A
NM_001321281.1:c.92+12G>A NP_001308210.1:n.92+12G>A
NM_001321281.2:c.92+12G>A NP_001308210.1:n.92+12G>A
NM_001321282.1:c.-1281+12G>A NP_001308211.1:n.-1281+12G>A
NM_001321282.2:c.-1281+12G>A NP_001308211.1:n.-1281+12G>A
NM_001321283.1:c.-75+12G>A NP_001308212.1:n.-75+12G>A
NM_001321283.2:c.-75+12G>A NP_001308212.1:n.-75+12G>A
NM_001321285.1:c.-238+12G>A NP_001308214.1:n.-238+12G>A
NM_001321285.2:c.-238+12G>A NP_001308214.1:n.-238+12G>A
NM_017636.3:c.92+12G>A NP_060106.2:n.92+12G>A
ENST00000252826.9:c.92+12G>A ENSP00000252826.4:n.92+12G>A
ENST00000427978.6:c.92+12G>A ENSP00000407492.1:n.92+12G>A
ENST00000595519.5:c.92+12G>A ENSP00000469893.1:n.92+12G>A
ENST00000596338.5:n.127+12G>A
ENST00000598502.5:c.92+12G>A ENSP00000470229.1:n.92+12G>A
ENST00000598691.5:c.92+12G>A ENSP00000473231.1:n.92+12G>A
ENST00000598697.5:c.92+12G>A ENSP00000468989.1:n.92+12G>A
ENST00000599628.5:c.*8G>A ENSP00000483753.1:n.*8G>A
XM_011527046.1:c.-75+12G>A XP_011525348.1:n.-75+12G>A