Canonical Allele Identifier: CA9569894

Gene: TRPM4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49210786A>C , CM000681.2:g.49210786A>C	GRCh38
NC_000019.9:g.49714043A>C , CM000681.1:g.49714043A>C	GRCh37
NC_000019.8:g.54405855A>C	NCBI36
NG_027551.1:g.58028A>C
NG_027551.2:g.58028A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252826.10:c.3405A>C MANE Select	ENSP00000252826.4:p.Ala1135=
ENST00000252826.9:c.3405A>C	ENSP00000252826.4:p.Ala1135=
ENST00000427978.6:c.2970A>C	ENSP00000407492.1:p.Ala990=
ENST00000595071.5:n.2369A>C
ENST00000595519.5:c.*2815A>C	ENSP00000469893.1:n.*2815A>C
ENST00000596338.5:n.3502A>C
ENST00000597316.1:c.53A>C
ENST00000598502.5:c.*2518A>C	ENSP00000470229.1:n.*2518A>C
ENST00000598697.5:c.*2360A>C	ENSP00000468989.1:n.*2360A>C
ENST00000599459.1:n.186A>C
NM_001195227.1:c.2970A>C	NP_001182156.1:p.Ala990=
NM_017636.3:c.3405A>C	NP_060106.2:p.Ala1135=
XM_005259017.1:c.2118A>C	XP_005259074.1:p.Ala706=
XM_005259018.2:c.1797A>C	XP_005259075.1:p.Ala599=
XM_011527046.1:c.2883A>C	XP_011525348.1:p.Ala961=
NM_001321281.1:c.3060A>C	NP_001308210.1:p.Ala1020=
NM_001321282.1:c.1797A>C	NP_001308211.1:p.Ala599=
NM_001321283.1:c.2883A>C	NP_001308212.1:p.Ala961=
NM_001321285.1:c.2343A>C	NP_001308214.1:p.Ala781=
XM_024451557.1:c.1431A>C	XP_024307325.1:p.Ala477=
NM_017636.4:c.3405A>C MANE Select	NP_060106.2:p.Ala1135=
NM_001195227.2:c.2970A>C	NP_001182156.1:p.Ala990=
NM_001321281.2:c.3060A>C	NP_001308210.1:p.Ala1020=
NM_001321282.2:c.1797A>C	NP_001308211.1:p.Ala599=
NM_001321283.2:c.2883A>C	NP_001308212.1:p.Ala961=
NM_001321285.2:c.2343A>C	NP_001308214.1:p.Ala781=