Canonical Allele Identifier: CA2340280656

Gene: TRPM4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49182608G= , CM000681.2:g.49182608G=	GRCh38
NC_000019.9:g.49685865G= , CM000681.1:g.49685865G=	GRCh37
NC_000019.8:g.54377677G=	NCBI36
NG_027551.1:g.29850G=
NG_027551.2:g.29850G=

Transcript Alleles

HGVS	Amino-acid Change
NM_017636.4:c.1294G= MANE Select	NP_060106.2:p.Ala432=
ENST00000252826.10:c.1294G= MANE Select	ENSP00000252826.4:p.Ala432=
NM_001195227.1:c.1294G=	NP_001182156.1:p.Ala432=
NM_001195227.2:c.1294G=	NP_001182156.1:p.Ala432=
NM_001321281.1:c.949G=	NP_001308210.1:p.Ala317=
NM_001321281.2:c.949G=	NP_001308210.1:p.Ala317=
NM_001321282.1:c.-260G=	NP_001308211.1:n.-260G=
NM_001321282.2:c.-260G=	NP_001308211.1:n.-260G=
NM_001321283.1:c.772G=	NP_001308212.1:p.Ala258=
NM_001321283.2:c.772G=	NP_001308212.1:p.Ala258=
NM_001321285.1:c.232G=	NP_001308214.1:p.Ala78=
NM_001321285.2:c.232G=	NP_001308214.1:p.Ala78=
NM_017636.3:c.1294G=	NP_060106.2:p.Ala432=
ENST00000252826.9:c.1294G=	ENSP00000252826.4:p.Ala432=
ENST00000427978.6:c.1294G=	ENSP00000407492.1:p.Ala432=
ENST00000595071.5:n.83G=
ENST00000595519.5:c.*704G=	ENSP00000469893.1:n.*704G=
ENST00000596338.5:n.1216G=
ENST00000598502.5:c.*462G=	ENSP00000470229.1:n.*462G=
ENST00000598697.5:c.*249G=	ENSP00000468989.1:n.*249G=
ENST00000601347.1:n.495G=
XM_005259017.1:c.7G=	XP_005259074.1:p.Ala3=
XM_011527046.1:c.772G=	XP_011525348.1:p.Ala258=
XM_024451557.1:c.-801G=	XP_024307325.1:n.-801G=