Canonical Allele Identifier: CA1081892568
Gene: TRPC7 HGNC NCBI
TRPC7-AS2 HGNC NCBI

Linked Data

dbSNP Id: rs1756113727

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136240122_136240124del , CM000667.2:g.136240122_136240124del GRCh38
NC_000005.9:g.135575810_135575812del , CM000667.1:g.135575810_135575812del GRCh37
NC_000005.8:g.135603709_135603711del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000352189.8:c.1496+7350_1496+7352del (TRPC7) ENSP00000330322.5:n.1496+7350_1496+7352del
ENST00000378459.7:c.1661+7350_1661+7352del (TRPC7) ENSP00000367720.3:n.1661+7350_1661+7352del
ENST00000502753.4:c.1679+7350_1679+7352del (TRPC7) ENSP00000424854.3:n.1679+7350_1679+7352del
ENST00000503275.6:c.*717+7350_*717+7352del (TRPC7) ENSP00000421571.2:n.*717+7350_*717+7352del
ENST00000513104.6:c.1844+7350_1844+7352del (TRPC7) MANE Select ENSP00000426070.2:n.1844+7350_1844+7352del
ENST00000352189.7:c.1496+7350_1496+7352del (TRPC7) ENSP00000330322.5:n.1496+7350_1496+7352del
ENST00000378459.6:c.1661+7350_1661+7352del (TRPC7) ENSP00000367720.3:n.1661+7350_1661+7352del
ENST00000502753.3:c.1679+7350_1679+7352del (TRPC7) ENSP00000424854.3:n.1679+7350_1679+7352del
ENST00000503275.5:c.1860+7350_1860+7352del (TRPC7) ENSP00000421571.2:n.1860+7350_1860+7352del
ENST00000513104.5:c.1844+7350_1844+7352del (TRPC7) ENSP00000426070.1:n.1844+7350_1844+7352del
ENST00000514963.5:c.1279+7350_1279+7352del (TRPC7) ENSP00000426870.2:n.1279+7350_1279+7352del
NM_001167576.1:c.1496+7350_1496+7352del (TRPC7) NP_001161048.1:n.1496+7350_1496+7352del
NM_001167577.1:c.1661+7350_1661+7352del (TRPC7) NP_001161049.1:n.1661+7350_1661+7352del
NM_020389.2:c.1844+7350_1844+7352del (TRPC7) NP_065122.1:n.1844+7350_1844+7352del
XM_011543516.1:c.1817+7350_1817+7352del (TRPC7) XP_011541818.1:n.1817+7350_1817+7352del
XM_011543517.1:c.1652+7350_1652+7352del (TRPC7) XP_011541819.1:n.1652+7350_1652+7352del
XM_011543518.1:c.1649+7350_1649+7352del (TRPC7) XP_011541820.1:n.1649+7350_1649+7352del
NR_133682.1:n.59+13409_59+13411del (TRPC7-AS2)
NM_001167576.2:c.1496+7350_1496+7352del (TRPC7) NP_001161048.1:n.1496+7350_1496+7352del
NM_001167577.2:c.1661+7350_1661+7352del (TRPC7) NP_001161049.1:n.1661+7350_1661+7352del
NM_001376901.1:c.1679+7350_1679+7352del (TRPC7) NP_001363830.1:n.1679+7350_1679+7352del
NM_020389.3:c.1844+7350_1844+7352del (TRPC7) MANE Select NP_065122.1:n.1844+7350_1844+7352del