Canonical Allele Identifier: CA10581544
Gene: TRPC6 HGNC NCBI

Linked Data

ClinVar Variation Id: 236172
ClinVar RCV Id: RCV000225052
dbSNP Id: rs878853199

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101483218A>G , CM000673.2:g.101483218A>G GRCh38
NC_000011.9:g.101353949A>G , CM000673.1:g.101353949A>G GRCh37
NC_000011.8:g.100859159A>G NCBI36
NG_011476.1:g.105711T>C
NG_011476.2:g.105711T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000344327.8:c.1294-53T>C MANE Select ENSP00000340913.3:n.1294-53T>C
ENST00000344327.7:c.1294-53T>C ENSP00000340913.3:n.1294-53T>C
ENST00000348423.8:c.946-53T>C ENSP00000343672.4:n.946-53T>C
ENST00000360497.4:c.1129-53T>C ENSP00000353687.4:n.1129-53T>C
ENST00000532133.5:c.1294-53T>C ENSP00000435574.1:n.1294-53T>C
NM_004621.5:c.1294-53T>C NP_004612.2:n.1294-53T>C
XM_006718898.2:c.1294-53T>C XP_006718961.1:n.1294-53T>C
XM_011542968.1:c.1129-53T>C XP_011541270.1:n.1129-53T>C
XM_011542969.1:c.1294-53T>C XP_011541271.1:n.1294-53T>C
XM_011542968.3:c.1129-53T>C XP_011541270.1:n.1129-53T>C
XM_017018221.2:c.946-53T>C XP_016873710.1:n.946-53T>C
XR_001747948.2:n.1650-53T>C
NM_004621.6:c.1294-53T>C MANE Select NP_004612.2:n.1294-53T>C