Canonical Allele Identifier: CA2340267847

Gene: TRPM4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49157891G= , CM000681.2:g.49157891G=	GRCh38
NC_000019.9:g.49661148G= , CM000681.1:g.49661148G=	GRCh37
NC_000019.8:g.54352960G=	NCBI36
NG_027551.1:g.5133G=
NG_027551.2:g.5133G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252826.10:c.24+1G= MANE Select	ENSP00000252826.4:n.24+1G=
ENST00000252826.9:c.24+1G=	ENSP00000252826.4:n.24+1G=
ENST00000427978.6:c.24+1G=	ENSP00000407492.1:n.24+1G=
ENST00000595519.5:c.24+1G=	ENSP00000469893.1:n.24+1G=
ENST00000596338.5:n.59+1G=
ENST00000598502.5:c.24+1G=	ENSP00000470229.1:n.24+1G=
ENST00000598691.5:c.24+1G=	ENSP00000473231.1:n.24+1G=
ENST00000598697.5:c.24+1G=	ENSP00000468989.1:n.24+1G=
ENST00000599628.5:c.24+1G=	ENSP00000483753.1:n.24+1G=
NM_001195227.1:c.24+1G=	NP_001182156.1:n.24+1G=
NM_017636.3:c.24+1G=	NP_060106.2:n.24+1G=
XM_011527046.1:c.-143+1G=	XP_011525348.1:n.-143+1G=
NM_001321281.1:c.24+1G=	NP_001308210.1:n.24+1G=
NM_001321282.1:c.-1349+1G=	NP_001308211.1:n.-1349+1G=
NM_001321283.1:c.-143+1G=	NP_001308212.1:n.-143+1G=
NM_001321285.1:c.-306+1G=	NP_001308214.1:n.-306+1G=
NM_017636.4:c.24+1G= MANE Select	NP_060106.2:n.24+1G=
NM_001195227.2:c.24+1G=	NP_001182156.1:n.24+1G=
NM_001321281.2:c.24+1G=	NP_001308210.1:n.24+1G=
NM_001321282.2:c.-1349+1G=	NP_001308211.1:n.-1349+1G=
NM_001321283.2:c.-143+1G=	NP_001308212.1:n.-143+1G=
NM_001321285.2:c.-306+1G=	NP_001308214.1:n.-306+1G=