Canonical Allele Identifier: CA2340283368

Gene: TRPM4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49188641G= , CM000681.2:g.49188641G=	GRCh38
NC_000019.9:g.49691898G= , CM000681.1:g.49691898G=	GRCh37
NC_000019.8:g.54383710G=	NCBI36
NG_027551.1:g.35883G=
NG_027551.2:g.35883G=

Transcript Alleles

HGVS	Amino-acid Change
NM_017636.4:c.1744G= MANE Select	NP_060106.2:p.Gly582=
ENST00000252826.10:c.1744G= MANE Select	ENSP00000252826.4:p.Gly582=
NM_001195227.1:c.1744G=	NP_001182156.1:p.Gly582=
NM_001195227.2:c.1744G=	NP_001182156.1:p.Gly582=
NM_001321281.1:c.1399G=	NP_001308210.1:p.Gly467=
NM_001321281.2:c.1399G=	NP_001308210.1:p.Gly467=
NM_001321282.1:c.136G=	NP_001308211.1:p.Gly46=
NM_001321282.2:c.136G=	NP_001308211.1:p.Gly46=
NM_001321283.1:c.1222G=	NP_001308212.1:p.Gly408=
NM_001321283.2:c.1222G=	NP_001308212.1:p.Gly408=
NM_001321285.1:c.682G=	NP_001308214.1:p.Gly228=
NM_001321285.2:c.682G=	NP_001308214.1:p.Gly228=
NM_017636.3:c.1744G=	NP_060106.2:p.Gly582=
ENST00000252826.9:c.1744G=	ENSP00000252826.4:p.Gly582=
ENST00000427978.6:c.1744G=	ENSP00000407492.1:p.Gly582=
ENST00000595071.5:n.533G=
ENST00000595519.5:c.*1154G=	ENSP00000469893.1:n.*1154G=
ENST00000596338.5:n.1666G=
ENST00000598502.5:c.*857G=	ENSP00000470229.1:n.*857G=
ENST00000598697.5:c.*699G=	ENSP00000468989.1:n.*699G=
XM_005259017.1:c.457G=	XP_005259074.1:p.Gly153=
XM_005259018.2:c.136G=	XP_005259075.1:p.Gly46=
XM_011527046.1:c.1222G=	XP_011525348.1:p.Gly408=
XM_024451557.1:c.-406G=	XP_024307325.1:n.-406G=