Canonical Allele Identifier: CA2176499941

Gene: TRPM7

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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