Canonical Allele Identifier: CA2839279889
Gene: TRPM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49157844dup , CM000681.2:g.49157844dup GRCh38
NC_000019.9:g.49661101dup , CM000681.1:g.49661101dup GRCh37
NC_000019.8:g.54352913dup NCBI36
NG_027551.1:g.5086dup
NG_027551.2:g.5086dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000252826.10:c.-23dup MANE Select ENSP00000252826.4:n.-23dup
ENST00000252826.9:c.-23dup ENSP00000252826.4:n.-23dup
ENST00000427978.6:c.-23dup ENSP00000407492.1:n.-23dup
ENST00000595519.5:c.-23dup ENSP00000469893.1:n.-23dup
ENST00000596338.5:n.13dup
ENST00000598502.5:c.-23dup ENSP00000470229.1:n.-23dup
ENST00000598691.5:c.-23dup ENSP00000473231.1:n.-23dup
ENST00000598697.5:c.-23dup ENSP00000468989.1:n.-23dup
ENST00000599628.5:c.-23dup ENSP00000483753.1:n.-23dup
NM_001195227.1:c.-23dup NP_001182156.1:n.-23dup
NM_017636.3:c.-23dup NP_060106.2:n.-23dup
XM_011527046.1:c.-189dup XP_011525348.1:n.-189dup
NM_001321281.1:c.-23dup NP_001308210.1:n.-23dup
NM_001321282.1:c.-1395dup NP_001308211.1:n.-1395dup
NM_001321283.1:c.-189dup NP_001308212.1:n.-189dup
NM_001321285.1:c.-352dup NP_001308214.1:n.-352dup
NM_017636.4:c.-23dup MANE Select NP_060106.2:n.-23dup
NM_001195227.2:c.-23dup NP_001182156.1:n.-23dup
NM_001321281.2:c.-23dup NP_001308210.1:n.-23dup
NM_001321282.2:c.-1395dup NP_001308211.1:n.-1395dup
NM_001321283.2:c.-189dup NP_001308212.1:n.-189dup
NM_001321285.2:c.-352dup NP_001308214.1:n.-352dup