Canonical Allele Identifier: CA918953730

Gene: TRPC6

Linked Data

• dbSNP Id: rs1555000695

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101488717_101488718insA , CM000673.2:g.101488717_101488718insA	GRCh38
NC_000011.9:g.101359448_101359449insA , CM000673.1:g.101359448_101359449insA	GRCh37
NC_000011.8:g.100864658_100864659insA	NCBI36
NG_011476.1:g.100211_100212insT
NG_011476.2:g.100211_100212insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344327.8:c.1293+219_1293+220insT MANE Select	ENSP00000340913.3:n.1293+219_1293+220insT
ENST00000344327.7:c.1293+219_1293+220insT	ENSP00000340913.3:n.1293+219_1293+220insT
ENST00000348423.8:c.946-5553_946-5552insT	ENSP00000343672.4:n.946-5553_946-5552insT
ENST00000360497.4:c.1128+2838_1128+2839insT	ENSP00000353687.4:n.1128+2838_1128+2839insT
ENST00000532133.5:c.1293+219_1293+220insT	ENSP00000435574.1:n.1293+219_1293+220insT
NM_004621.5:c.1293+219_1293+220insT	NP_004612.2:n.1293+219_1293+220insT
XM_006718898.2:c.1293+219_1293+220insT	XP_006718961.1:n.1293+219_1293+220insT
XM_011542968.1:c.1128+219_1128+220insT	XP_011541270.1:n.1128+219_1128+220insT
XM_011542969.1:c.1293+219_1293+220insT	XP_011541271.1:n.1293+219_1293+220insT
XM_011542968.3:c.1128+219_1128+220insT	XP_011541270.1:n.1128+219_1128+220insT
XM_017018221.2:c.946-5553_946-5552insT	XP_016873710.1:n.946-5553_946-5552insT
XR_001747948.2:n.1649+219_1649+220insT
NM_004621.6:c.1293+219_1293+220insT MANE Select	NP_004612.2:n.1293+219_1293+220insT