Canonical Allele Identifier: CA7556930
Gene: TRPM7 HGNC NCBI
MyVariant.info:
GRCh38 chr15:g.50586377G>A
GRCh37 chr15:g.50878574G>A
gnomAD v2:
15:50878574 G / A
gnomAD v3:
15:50586377 G / A
gnomAD v4:
chr15-50586377-G-A
Joint Max Group AF 0.50296452 (AMR)
Genomes Max Group AF 0.47999252 (AMR)
Exomes Max Group AF 0.50859807 (AMR)
dbSNP:
3109894
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.50586377G>A , CM000677.2:g.50586377G>A GRCh38
NC_000015.9:g.50878574G>A , CM000677.1:g.50878574G>A GRCh37
NC_000015.8:g.48665866G>A NCBI36
NG_021363.1:g.105439C>T
NG_021363.2:g.105439C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000645282.1:n.290+15C>T
ENST00000646667.1:c.4486+15C>T MANE Select ENSP00000495860.1:n.4486+15C>T
ENST00000313478.11:c.4486+15C>T ENSP00000320239.7:n.4486+15C>T
ENST00000560849.2:n.191+15C>T
ENST00000560955.5:c.4486+15C>T ENSP00000453277.1:n.4486+15C>T
NM_001301212.1:c.4486+15C>T NP_001288141.1:n.4486+15C>T
NM_017672.5:c.4486+15C>T NP_060142.3:n.4486+15C>T
XM_005254486.2:c.4546+15C>T XP_005254543.1:n.4546+15C>T
XM_005254487.2:c.4546+15C>T XP_005254544.1:n.4546+15C>T
XR_931853.1:n.4828+15C>T
NR_149152.1:n.4718+15C>T
NR_149153.1:n.4641+15C>T
NR_149154.1:n.4568+15C>T
XM_005254486.4:c.4546+15C>T XP_005254543.1:n.4546+15C>T
XM_017022350.1:c.4573+15C>T XP_016877839.1:n.4573+15C>T
XM_017022351.1:c.4573+15C>T XP_016877840.1:n.4573+15C>T
XM_017022352.1:c.4513+15C>T XP_016877841.1:n.4513+15C>T
XM_017022353.2:c.4513+15C>T XP_016877842.1:n.4513+15C>T
XM_017022354.1:c.4369+15C>T XP_016877843.1:n.4369+15C>T
XM_017022355.1:c.4369+15C>T XP_016877844.1:n.4369+15C>T
XR_001751325.1:n.4588+15C>T
XR_001751326.2:n.4588+15C>T
XR_001751327.1:n.4588+15C>T
XR_001751328.2:n.4588+15C>T
XR_002957654.1:n.4478+15C>T
NM_017672.6:c.4486+15C>T MANE Select NP_060142.3:n.4486+15C>T
NM_001301212.2:c.4486+15C>T NP_001288141.1:n.4486+15C>T
NR_149152.2:n.4700+15C>T
NR_149153.2:n.4623+15C>T
NR_149154.2:n.4550+15C>T
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