Canonical Allele Identifier: CA14080075

Gene: TRPM7

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50675526T>C , CM000677.2:g.50675526T>C	GRCh38
NC_000015.9:g.50967723T>C , CM000677.1:g.50967723T>C	GRCh37
NC_000015.8:g.48755015T>C	NCBI36
NG_021363.1:g.16290A>G
NG_021363.2:g.16290A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646667.1:c.3+11005A>G MANE Select	ENSP00000495860.1:n.3+11005A>G
ENST00000676296.1:c.187+11005A>G	ENSP00000502268.1:n.187+11005A>G
ENST00000313478.11:c.3+11005A>G	ENSP00000320239.7:n.3+11005A>G
ENST00000560955.5:c.3+11005A>G	ENSP00000453277.1:n.3+11005A>G
NM_001301212.1:c.3+11005A>G	NP_001288141.1:n.3+11005A>G
NM_017672.5:c.3+11005A>G	NP_060142.3:n.3+11005A>G
XM_005254486.2:c.3+11005A>G	XP_005254543.1:n.3+11005A>G
XM_005254487.2:c.3+11005A>G	XP_005254544.1:n.3+11005A>G
XM_011521712.1:c.3+11005A>G	XP_011520014.1:n.3+11005A>G
XR_931853.1:n.285+11005A>G
NR_149152.1:n.285+11005A>G
NR_149153.1:n.285+11005A>G
NR_149154.1:n.285+11005A>G
XM_005254486.4:c.3+11005A>G	XP_005254543.1:n.3+11005A>G
XM_017022354.1:c.-244A>G	XP_016877843.1:n.-244A>G
NM_017672.6:c.3+11005A>G MANE Select	NP_060142.3:n.3+11005A>G
NM_001301212.2:c.3+11005A>G	NP_001288141.1:n.3+11005A>G
NR_149152.2:n.267+11005A>G
NR_149153.2:n.267+11005A>G
NR_149154.2:n.267+11005A>G