Canonical Allele Identifier: CA2176474885

Gene: TRPM7

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50590626A= , CM000677.2:g.50590626A=	GRCh38
NC_000015.9:g.50882823A= , CM000677.1:g.50882823A=	GRCh37
NC_000015.8:g.48670115A=	NCBI36
NG_021363.1:g.101190T=
NG_021363.2:g.101190T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645282.1:n.129-970T=
ENST00000646667.1:c.4325-970T= MANE Select	ENSP00000495860.1:n.4325-970T=
ENST00000313478.11:c.4325-970T=	ENSP00000320239.7:n.4325-970T=
ENST00000560955.5:c.4325-970T=	ENSP00000453277.1:n.4325-970T=
NM_001301212.1:c.4325-970T=	NP_001288141.1:n.4325-970T=
NM_017672.5:c.4325-970T=	NP_060142.3:n.4325-970T=
XM_005254486.2:c.4325-970T=	XP_005254543.1:n.4325-970T=
XM_005254487.2:c.4325-970T=	XP_005254544.1:n.4325-970T=
XR_931853.1:n.4607-970T=
NR_149152.1:n.4557-970T=
NR_149153.1:n.4480-970T=
NR_149154.1:n.4407-970T=
XM_005254486.4:c.4325-970T=	XP_005254543.1:n.4325-970T=
XM_017022350.1:c.4352-970T=	XP_016877839.1:n.4352-970T=
XM_017022351.1:c.4352-970T=	XP_016877840.1:n.4352-970T=
XM_017022352.1:c.4352-970T=	XP_016877841.1:n.4352-970T=
XM_017022353.2:c.4352-970T=	XP_016877842.1:n.4352-970T=
XM_017022354.1:c.4148-970T=	XP_016877843.1:n.4148-970T=
XM_017022355.1:c.4148-970T=	XP_016877844.1:n.4148-970T=
XR_001751325.1:n.4367-970T=
XR_001751326.2:n.4367-970T=
XR_001751327.1:n.4367-970T=
XR_001751328.2:n.4367-970T=
XR_002957653.1:n.5230-970T=
XR_002957654.1:n.4317-970T=
NM_017672.6:c.4325-970T= MANE Select	NP_060142.3:n.4325-970T=
NM_001301212.2:c.4325-970T=	NP_001288141.1:n.4325-970T=
NR_149152.2:n.4539-970T=
NR_149153.2:n.4462-970T=
NR_149154.2:n.4389-970T=