Canonical Allele Identifier: CA10581549

Gene: TRPC6

Linked Data

• ClinVar Variation Id: 236177
• ClinVar RCV Id: RCV000225018
• dbSNP Id: rs878853204
• MyVariant Identifiers: chr11:g.101374580T>A (hg19) ; chr11:g.101503849T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101503849T>A , CM000673.2:g.101503849T>A	GRCh38
NC_000011.9:g.101374580T>A , CM000673.1:g.101374580T>A	GRCh37
NC_000011.8:g.100879790T>A	NCBI36
NG_011476.1:g.85080A>T
NG_011476.2:g.85080A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344327.8:c.945+175A>T MANE Select	ENSP00000340913.3:n.945+175A>T
ENST00000344327.7:c.945+175A>T	ENSP00000340913.3:n.945+175A>T
ENST00000348423.8:c.945+175A>T	ENSP00000343672.4:n.945+175A>T
ENST00000360497.4:c.945+175A>T	ENSP00000353687.4:n.945+175A>T
ENST00000527240.1:n.67+175A>T
ENST00000532133.5:c.945+175A>T	ENSP00000435574.1:n.945+175A>T
NM_004621.5:c.945+175A>T	NP_004612.2:n.945+175A>T
XM_006718898.2:c.945+175A>T	XP_006718961.1:n.945+175A>T
XM_011542968.1:c.780+175A>T	XP_011541270.1:n.780+175A>T
XM_011542969.1:c.945+175A>T	XP_011541271.1:n.945+175A>T
XM_011542968.3:c.780+175A>T	XP_011541270.1:n.780+175A>T
XM_017018221.2:c.945+175A>T	XP_016873710.1:n.945+175A>T
XR_001747948.2:n.1301+175A>T
NM_004621.6:c.945+175A>T MANE Select	NP_004612.2:n.945+175A>T