Canonical Allele Identifier: CA9568935

Gene: TRPM4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49168695G>A , CM000681.2:g.49168695G>A	GRCh38
NC_000019.9:g.49671952G>A , CM000681.1:g.49671952G>A	GRCh37
NC_000019.8:g.54363764G>A	NCBI36
NG_027551.1:g.15937G>A
NG_027551.2:g.15937G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252826.10:c.755G>A MANE Select	ENSP00000252826.4:p.Arg252His
ENST00000252826.9:c.755G>A	ENSP00000252826.4:p.Arg252His
ENST00000427978.6:c.755G>A	ENSP00000407492.1:p.Arg252His
ENST00000595519.5:c.*165G>A	ENSP00000469893.1:n.*165G>A
ENST00000596338.5:n.790G>A
ENST00000598502.5:c.574G>A	ENSP00000470229.1:p.Ala192Thr
ENST00000598691.5:c.410G>A	ENSP00000473231.1:p.Arg137His
ENST00000598697.5:c.235G>A	ENSP00000468989.1:p.Ala79Thr
ENST00000601347.1:n.69G>A
NM_001195227.1:c.755G>A	NP_001182156.1:p.Arg252His
NM_017636.3:c.755G>A	NP_060106.2:p.Arg252His
XM_005259017.1:c.-420G>A	XP_005259074.1:n.-420G>A
XM_011527046.1:c.233G>A	XP_011525348.1:p.Arg78His
NM_001321281.1:c.410G>A	NP_001308210.1:p.Arg137His
NM_001321282.1:c.-799G>A	NP_001308211.1:n.-799G>A
NM_001321283.1:c.233G>A	NP_001308212.1:p.Arg78His
NM_001321285.1:c.-95G>A	NP_001308214.1:n.-95G>A
XM_024451557.1:c.-1340G>A	XP_024307325.1:n.-1340G>A
NM_017636.4:c.755G>A MANE Select	NP_060106.2:p.Arg252His
NM_001195227.2:c.755G>A	NP_001182156.1:p.Arg252His
NM_001321281.2:c.410G>A	NP_001308210.1:p.Arg137His
NM_001321282.2:c.-799G>A	NP_001308211.1:n.-799G>A
NM_001321283.2:c.233G>A	NP_001308212.1:p.Arg78His
NM_001321285.2:c.-95G>A	NP_001308214.1:n.-95G>A