Canonical Allele Identifier: CA392405094

Gene: TRPM7

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50599148C>T , CM000677.2:g.50599148C>T	GRCh38
NC_000015.9:g.50891345C>T , CM000677.1:g.50891345C>T	GRCh37
NC_000015.8:g.48678637C>T	NCBI36
NG_021363.1:g.92668G>A
NG_021363.2:g.92668G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_017672.6:c.3137G>A MANE Select	NP_060142.3:p.Gly1046Asp
ENST00000646667.1:c.3137G>A MANE Select	ENSP00000495860.1:p.Gly1046Asp
NM_001301212.1:c.3137G>A	NP_001288141.1:p.Gly1046Asp
NM_001301212.2:c.3137G>A	NP_001288141.1:p.Gly1046Asp
NM_017672.5:c.3137G>A	NP_060142.3:p.Gly1046Asp
NR_149152.1:n.3369G>A
NR_149152.2:n.3351G>A
NR_149153.1:n.3419G>A
NR_149153.2:n.3401G>A
NR_149154.1:n.3346G>A
NR_149154.2:n.3328G>A
ENST00000313478.11:c.3137G>A	ENSP00000320239.7:p.Gly1046Asp
ENST00000560284.1:n.518G>A
ENST00000560955.5:c.3137G>A	ENSP00000453277.1:p.Gly1046Asp
XM_005254486.2:c.3137G>A	XP_005254543.1:p.Gly1046Asp
XM_005254486.4:c.3137G>A	XP_005254543.1:p.Gly1046Asp
XM_005254487.2:c.3137G>A	XP_005254544.1:p.Gly1046Asp
XM_011521712.1:c.*60G>A	XP_011520014.1:n.*60G>A
XM_017022350.1:c.3164G>A	XP_016877839.1:p.Gly1055Asp
XM_017022351.1:c.3164G>A	XP_016877840.1:p.Gly1055Asp
XM_017022352.1:c.3164G>A	XP_016877841.1:p.Gly1055Asp
XM_017022353.2:c.3164G>A	XP_016877842.1:p.Gly1055Asp
XM_017022354.1:c.2960G>A	XP_016877843.1:p.Gly987Asp
XM_017022355.1:c.2960G>A	XP_016877844.1:p.Gly987Asp
XR_001751325.1:n.3179G>A
XR_001751326.2:n.3179G>A
XR_001751327.1:n.3179G>A
XR_001751328.2:n.3179G>A
XR_002957653.1:n.3179G>A
XR_002957654.1:n.3129G>A
XR_931853.1:n.3419G>A