Canonical Allele Identifier: CA10581534

Gene: TRPC6

Linked Data

• ClinVar Variation Id: 236161
• ClinVar RCV Id: RCV000225054
• dbSNP Id: rs878853189
• MyVariant Identifiers: chr11:g.101340254A>G (hg19) ; chr11:g.101469523A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101469523A>G , CM000673.2:g.101469523A>G	GRCh38
NC_000011.9:g.101340254A>G , CM000673.1:g.101340254A>G	GRCh37
NC_000011.8:g.100845464A>G	NCBI36
NG_011476.1:g.119406T>C
NG_011476.2:g.119406T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344327.8:c.2410-22T>C MANE Select	ENSP00000340913.3:n.2410-22T>C
ENST00000344327.7:c.2410-22T>C	ENSP00000340913.3:n.2410-22T>C
ENST00000348423.8:c.2062-22T>C	ENSP00000343672.4:n.2062-22T>C
ENST00000360497.4:c.2245-22T>C	ENSP00000353687.4:n.2245-22T>C
ENST00000532133.5:c.2176-22T>C	ENSP00000435574.1:n.2176-22T>C
NM_004621.5:c.2410-22T>C	NP_004612.2:n.2410-22T>C
XM_006718898.2:c.2409+1660T>C	XP_006718961.1:n.2409+1660T>C
XM_011542968.1:c.2245-22T>C	XP_011541270.1:n.2245-22T>C
XM_011542969.1:c.2410-22T>C	XP_011541271.1:n.2410-22T>C
XM_011542968.3:c.2245-22T>C	XP_011541270.1:n.2245-22T>C
XM_017018221.2:c.2062-22T>C	XP_016873710.1:n.2062-22T>C
XR_001747948.2:n.2766-22T>C
NM_004621.6:c.2410-22T>C MANE Select	NP_004612.2:n.2410-22T>C