Allele Registry

Canonical Allele Identifier: CA10581529

Gene: TRPC6 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr11:g.101455115A>G

GRCh37 chr11:g.101325846A>G

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000225085

ClinVar Variation:

236156

dbSNP:

878853184

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101455115A>G , CM000673.2:g.101455115A>G	GRCh38
NC_000011.9:g.101325846A>G , CM000673.1:g.101325846A>G	GRCh37
NC_000011.8:g.100831056A>G	NCBI36
NG_011476.1:g.133814T>C
NG_011476.2:g.133814T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344327.8:c.2485-14T>C MANE Select	ENSP00000340913.3:n.2485-14T>C
ENST00000344327.7:c.2485-14T>C	ENSP00000340913.3:n.2485-14T>C
ENST00000348423.8:c.2137-14T>C	ENSP00000343672.4:n.2137-14T>C
ENST00000360497.4:c.2320-14T>C	ENSP00000353687.4:n.2320-14T>C
ENST00000532133.5:c.2251-14T>C	ENSP00000435574.1:n.2251-14T>C
ENST00000532184.1:n.463T>C
NM_004621.5:c.2485-14T>C	NP_004612.2:n.2485-14T>C
XM_006718898.2:c.2410-14T>C	XP_006718961.1:n.2410-14T>C
XM_011542968.1:c.2320-14T>C	XP_011541270.1:n.2320-14T>C
XM_011542969.1:c.2482-10T>C	XP_011541271.1:n.2482-10T>C
XM_011542968.3:c.2320-14T>C	XP_011541270.1:n.2320-14T>C
XM_017018221.2:c.2137-14T>C	XP_016873710.1:n.2137-14T>C
XR_001747948.2:n.2838-10T>C
NM_004621.6:c.2485-14T>C MANE Select	NP_004612.2:n.2485-14T>C

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