Canonical Allele Identifier: CA2176521838

Gene: TRPM7

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50660478C= , CM000677.2:g.50660478C=	GRCh38
NC_000015.9:g.50952675C= , CM000677.1:g.50952675C=	GRCh37
NC_000015.8:g.48739967C=	NCBI36
NG_021363.1:g.31338G=
NG_021363.2:g.31338G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000646667.1:c.83+2489G= MANE Select	ENSP00000495860.1:n.83+2489G=
ENST00000676296.1:c.267+2489G=	ENSP00000502268.1:n.267+2489G=
ENST00000313478.11:c.83+2489G=	ENSP00000320239.7:n.83+2489G=
ENST00000560955.5:c.83+2489G=	ENSP00000453277.1:n.83+2489G=
NM_001301212.1:c.83+2489G=	NP_001288141.1:n.83+2489G=
NM_017672.5:c.83+2489G=	NP_060142.3:n.83+2489G=
XM_005254486.2:c.83+2489G=	XP_005254543.1:n.83+2489G=
XM_005254487.2:c.83+2489G=	XP_005254544.1:n.83+2489G=
XM_011521712.1:c.83+2489G=	XP_011520014.1:n.83+2489G=
XR_931853.1:n.365+2489G=
NR_149152.1:n.365+2489G=
NR_149153.1:n.365+2489G=
NR_149154.1:n.365+2489G=
XM_005254486.4:c.83+2489G=	XP_005254543.1:n.83+2489G=
XM_017022350.1:c.110+2489G=	XP_016877839.1:n.110+2489G=
XM_017022351.1:c.110+2489G=	XP_016877840.1:n.110+2489G=
XM_017022352.1:c.110+2489G=	XP_016877841.1:n.110+2489G=
XM_017022353.2:c.110+2489G=	XP_016877842.1:n.110+2489G=
XM_017022354.1:c.-95+2489G=	XP_016877843.1:n.-95+2489G=
XR_001751325.1:n.125+2489G=
XR_001751326.2:n.125+2489G=
XR_001751327.1:n.125+2489G=
XR_001751328.2:n.125+2489G=
XR_002957653.1:n.125+2489G=
XR_002957654.1:n.125+2489G=
NM_017672.6:c.83+2489G= MANE Select	NP_060142.3:n.83+2489G=
NM_001301212.2:c.83+2489G=	NP_001288141.1:n.83+2489G=
NR_149152.2:n.347+2489G=
NR_149153.2:n.347+2489G=
NR_149154.2:n.347+2489G=