Canonical Allele Identifier: CA670792861

Gene: TRPC6

Linked Data

• dbSNP Id: rs1341908440
• gnomAD v3: 11-101488806-A-G
• gnomAD v4: 11-101488806-A-G
• MyVariant Identifiers: chr11:g.101359537A>G (hg19) ; chr11:g.101488806A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101488806A>G , CM000673.2:g.101488806A>G	GRCh38
NC_000011.9:g.101359537A>G , CM000673.1:g.101359537A>G	GRCh37
NC_000011.8:g.100864747A>G	NCBI36
NG_011476.1:g.100123T>C
NG_011476.2:g.100123T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344327.8:c.1293+131T>C MANE Select	ENSP00000340913.3:n.1293+131T>C
ENST00000344327.7:c.1293+131T>C	ENSP00000340913.3:n.1293+131T>C
ENST00000348423.8:c.946-5641T>C	ENSP00000343672.4:n.946-5641T>C
ENST00000360497.4:c.1128+2750T>C	ENSP00000353687.4:n.1128+2750T>C
ENST00000532133.5:c.1293+131T>C	ENSP00000435574.1:n.1293+131T>C
NM_004621.5:c.1293+131T>C	NP_004612.2:n.1293+131T>C
XM_006718898.2:c.1293+131T>C	XP_006718961.1:n.1293+131T>C
XM_011542968.1:c.1128+131T>C	XP_011541270.1:n.1128+131T>C
XM_011542969.1:c.1293+131T>C	XP_011541271.1:n.1293+131T>C
XM_011542968.3:c.1128+131T>C	XP_011541270.1:n.1128+131T>C
XM_017018221.2:c.946-5641T>C	XP_016873710.1:n.946-5641T>C
XR_001747948.2:n.1649+131T>C
NM_004621.6:c.1293+131T>C MANE Select	NP_004612.2:n.1293+131T>C