Canonical Allele Identifier: CA9568832
Gene: TRPM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49168246C>T , CM000681.2:g.49168246C>T GRCh38
NC_000019.9:g.49671503C>T , CM000681.1:g.49671503C>T GRCh37
NC_000019.8:g.54363315C>T NCBI36
NG_027551.1:g.15488C>T
NG_027551.2:g.15488C>T

Transcript Alleles

HGVS Amino-acid Change
NM_017636.4:c.449-14C>T MANE Select NP_060106.2:n.449-14C>T
ENST00000252826.10:c.449-14C>T MANE Select ENSP00000252826.4:n.449-14C>T
NM_001195227.1:c.449-14C>T NP_001182156.1:n.449-14C>T
NM_001195227.2:c.449-14C>T NP_001182156.1:n.449-14C>T
NM_001321281.1:c.268-307C>T NP_001308210.1:n.268-307C>T
NM_001321281.2:c.268-307C>T NP_001308210.1:n.268-307C>T
NM_001321282.1:c.-1105-14C>T NP_001308211.1:n.-1105-14C>T
NM_001321282.2:c.-1105-14C>T NP_001308211.1:n.-1105-14C>T
NM_001321283.1:c.-74-14C>T NP_001308212.1:n.-74-14C>T
NM_001321283.2:c.-74-14C>T NP_001308212.1:n.-74-14C>T
NM_001321285.1:c.-237-307C>T NP_001308214.1:n.-237-307C>T
NM_001321285.2:c.-237-307C>T NP_001308214.1:n.-237-307C>T
NM_017636.3:c.449-14C>T NP_060106.2:n.449-14C>T
ENST00000252826.9:c.449-14C>T ENSP00000252826.4:n.449-14C>T
ENST00000427978.6:c.449-14C>T ENSP00000407492.1:n.449-14C>T
ENST00000594568.1:n.455-14C>T
ENST00000595519.5:c.93-14C>T ENSP00000469893.1:n.93-14C>T
ENST00000596338.5:n.484-14C>T
ENST00000598502.5:c.268-14C>T ENSP00000470229.1:n.268-14C>T
ENST00000598691.5:c.268-307C>T ENSP00000473231.1:n.268-307C>T
ENST00000598697.5:c.93-307C>T ENSP00000468989.1:n.93-307C>T
XM_011527046.1:c.-74-14C>T XP_011525348.1:n.-74-14C>T