Canonical Allele Identifier: CA14131716
Gene: TRPM7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.50597427G>C , CM000677.2:g.50597427G>C GRCh38
NC_000015.9:g.50889624G>C , CM000677.1:g.50889624G>C GRCh37
NC_000015.8:g.48676916G>C NCBI36
NG_021363.1:g.94389C>G
NG_021363.2:g.94389C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000646667.1:c.3164-1046C>G MANE Select ENSP00000495860.1:n.3164-1046C>G
ENST00000313478.11:c.3164-1046C>G ENSP00000320239.7:n.3164-1046C>G
ENST00000560284.1:n.545-1046C>G
ENST00000560955.5:c.3164-1046C>G ENSP00000453277.1:n.3164-1046C>G
NM_001301212.1:c.3164-1046C>G NP_001288141.1:n.3164-1046C>G
NM_017672.5:c.3164-1046C>G NP_060142.3:n.3164-1046C>G
XM_005254486.2:c.3164-1046C>G XP_005254543.1:n.3164-1046C>G
XM_005254487.2:c.3164-1046C>G XP_005254544.1:n.3164-1046C>G
XR_931853.1:n.3446-1046C>G
NR_149152.1:n.3396-1046C>G
NR_149153.1:n.3445+1695C>G
NR_149154.1:n.3372+1695C>G
XM_005254486.4:c.3164-1046C>G XP_005254543.1:n.3164-1046C>G
XM_017022350.1:c.3191-1046C>G XP_016877839.1:n.3191-1046C>G
XM_017022351.1:c.3191-1046C>G XP_016877840.1:n.3191-1046C>G
XM_017022352.1:c.3191-1046C>G XP_016877841.1:n.3191-1046C>G
XM_017022353.2:c.3191-1046C>G XP_016877842.1:n.3191-1046C>G
XM_017022354.1:c.2987-1046C>G XP_016877843.1:n.2987-1046C>G
XM_017022355.1:c.2987-1046C>G XP_016877844.1:n.2987-1046C>G
XR_001751325.1:n.3206-1046C>G
XR_001751326.2:n.3206-1046C>G
XR_001751327.1:n.3206-1046C>G
XR_001751328.2:n.3206-1046C>G
XR_002957653.1:n.3205+1695C>G
XR_002957654.1:n.3156-1046C>G
NM_017672.6:c.3164-1046C>G MANE Select NP_060142.3:n.3164-1046C>G
NM_001301212.2:c.3164-1046C>G NP_001288141.1:n.3164-1046C>G
NR_149152.2:n.3378-1046C>G
NR_149153.2:n.3427+1695C>G
NR_149154.2:n.3354+1695C>G
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