Canonical Allele Identifier: CA14080048
Gene: TRPM7 HGNC NCBI

Linked Data

dbSNP Id: rs7173321
gnomAD v2: 15-50922600-C-G
gnomAD v3: 15-50630403-C-G
gnomAD v4: 15-50630403-C-G
MyVariant Identifiers: chr15:g.50922600C>G (hg19) chr15:g.50630403C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.50630403C>G , CM000677.2:g.50630403C>G GRCh38
NC_000015.9:g.50922600C>G , CM000677.1:g.50922600C>G GRCh37
NC_000015.8:g.48709892C>G NCBI36
NG_021363.1:g.61413G>C
NG_021363.2:g.61413G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000646667.1:c.1204+1014G>C MANE Select ENSP00000495860.1:n.1204+1014G>C
ENST00000313478.11:c.1204+1014G>C ENSP00000320239.7:n.1204+1014G>C
ENST00000560955.5:c.1204+1014G>C ENSP00000453277.1:n.1204+1014G>C
NM_001301212.1:c.1204+1014G>C NP_001288141.1:n.1204+1014G>C
NM_017672.5:c.1204+1014G>C NP_060142.3:n.1204+1014G>C
XM_005254486.2:c.1204+1014G>C XP_005254543.1:n.1204+1014G>C
XM_005254487.2:c.1204+1014G>C XP_005254544.1:n.1204+1014G>C
XM_011521712.1:c.1204+1014G>C XP_011520014.1:n.1204+1014G>C
XR_931853.1:n.1486+1014G>C
NR_149152.1:n.1486+1014G>C
NR_149153.1:n.1486+1014G>C
NR_149154.1:n.1486+1014G>C
XM_005254486.4:c.1204+1014G>C XP_005254543.1:n.1204+1014G>C
XM_017022350.1:c.1231+1014G>C XP_016877839.1:n.1231+1014G>C
XM_017022351.1:c.1231+1014G>C XP_016877840.1:n.1231+1014G>C
XM_017022352.1:c.1231+1014G>C XP_016877841.1:n.1231+1014G>C
XM_017022353.2:c.1231+1014G>C XP_016877842.1:n.1231+1014G>C
XM_017022354.1:c.1027+1014G>C XP_016877843.1:n.1027+1014G>C
XM_017022355.1:c.1027+1014G>C XP_016877844.1:n.1027+1014G>C
XR_001751325.1:n.1246+1014G>C
XR_001751326.2:n.1246+1014G>C
XR_001751327.1:n.1246+1014G>C
XR_001751328.2:n.1246+1014G>C
XR_002957653.1:n.1246+1014G>C
XR_002957654.1:n.1246+1014G>C
NM_017672.6:c.1204+1014G>C MANE Select NP_060142.3:n.1204+1014G>C
NM_001301212.2:c.1204+1014G>C NP_001288141.1:n.1204+1014G>C
NR_149152.2:n.1468+1014G>C
NR_149153.2:n.1468+1014G>C
NR_149154.2:n.1468+1014G>C
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