Canonical Allele Identifier: CA349490

Gene: TRPM4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49167971C>T , CM000681.2:g.49167971C>T	GRCh38
NC_000019.9:g.49671228C>T , CM000681.1:g.49671228C>T	GRCh37
NC_000019.8:g.54363040C>T	NCBI36
NG_027551.1:g.15213C>T
NG_027551.2:g.15213C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252826.10:c.322C>T MANE Select	ENSP00000252826.4:p.Arg108Cys
ENST00000252826.9:c.322C>T	ENSP00000252826.4:p.Arg108Cys
ENST00000427978.6:c.322C>T	ENSP00000407492.1:p.Arg108Cys
ENST00000594568.1:n.328C>T
ENST00000595519.5:c.93-289C>T	ENSP00000469893.1:n.93-289C>T
ENST00000596338.5:n.357C>T
ENST00000598502.5:c.268-289C>T	ENSP00000470229.1:n.268-289C>T
ENST00000598691.5:c.268-582C>T	ENSP00000473231.1:n.268-582C>T
ENST00000598697.5:c.93-582C>T	ENSP00000468989.1:n.93-582C>T
NM_001195227.1:c.322C>T	NP_001182156.1:p.Arg108Cys
NM_017636.3:c.322C>T	NP_060106.2:p.Arg108Cys
XM_011527046.1:c.-74-289C>T	XP_011525348.1:n.-74-289C>T
NM_001321281.1:c.268-582C>T	NP_001308210.1:n.268-582C>T
NM_001321282.1:c.-1105-289C>T	NP_001308211.1:n.-1105-289C>T
NM_001321283.1:c.-74-289C>T	NP_001308212.1:n.-74-289C>T
NM_001321285.1:c.-237-582C>T	NP_001308214.1:n.-237-582C>T
NM_017636.4:c.322C>T MANE Select	NP_060106.2:p.Arg108Cys
NM_001195227.2:c.322C>T	NP_001182156.1:p.Arg108Cys
NM_001321281.2:c.268-582C>T	NP_001308210.1:n.268-582C>T
NM_001321282.2:c.-1105-289C>T	NP_001308211.1:n.-1105-289C>T
NM_001321283.2:c.-74-289C>T	NP_001308212.1:n.-74-289C>T
NM_001321285.2:c.-237-582C>T	NP_001308214.1:n.-237-582C>T