Canonical Allele Identifier: CA2586334976
Gene: TRPM4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49157809G>C , CM000681.2:g.49157809G>C GRCh38
NC_000019.9:g.49661066G>C , CM000681.1:g.49661066G>C GRCh37
NC_000019.8:g.54352878G>C NCBI36
NG_027551.1:g.5051G>C
NG_027551.2:g.5051G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252826.10:c.-58G>C MANE Select ENSP00000252826.4:n.-58G>C
ENST00000252826.9:c.-58G>C ENSP00000252826.4:n.-58G>C
ENST00000595519.5:c.-58G>C ENSP00000469893.1:n.-58G>C
ENST00000598691.5:c.-58G>C ENSP00000473231.1:n.-58G>C
ENST00000598697.5:c.-58G>C ENSP00000468989.1:n.-58G>C
ENST00000599628.5:c.-58G>C ENSP00000483753.1:n.-58G>C
NM_001195227.1:c.-58G>C NP_001182156.1:n.-58G>C
NM_017636.3:c.-58G>C NP_060106.2:n.-58G>C
XM_011527046.1:c.-224G>C XP_011525348.1:n.-224G>C
NM_001321281.1:c.-58G>C NP_001308210.1:n.-58G>C
NM_001321282.1:c.-1430G>C NP_001308211.1:n.-1430G>C
NM_001321283.1:c.-224G>C NP_001308212.1:n.-224G>C
NM_001321285.1:c.-387G>C NP_001308214.1:n.-387G>C
NM_017636.4:c.-58G>C MANE Select NP_060106.2:n.-58G>C
NM_001195227.2:c.-58G>C NP_001182156.1:n.-58G>C
NM_001321281.2:c.-58G>C NP_001308210.1:n.-58G>C
NM_001321282.2:c.-1430G>C NP_001308211.1:n.-1430G>C
NM_001321283.2:c.-224G>C NP_001308212.1:n.-224G>C
NM_001321285.2:c.-387G>C NP_001308214.1:n.-387G>C