Canonical Allele Identifier: CA10581530

Gene: TRPC6

Linked Data

• ClinVar Variation Id: 236157
• ClinVar RCV Id: RCV000225029
• dbSNP Id: rs878853185
• MyVariant Identifiers: chr11:g.101325876T>C (hg19) ; chr11:g.101455145T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101455145T>C , CM000673.2:g.101455145T>C	GRCh38
NC_000011.9:g.101325876T>C , CM000673.1:g.101325876T>C	GRCh37
NC_000011.8:g.100831086T>C	NCBI36
NG_011476.1:g.133784A>G
NG_011476.2:g.133784A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344327.8:c.2485-44A>G MANE Select	ENSP00000340913.3:n.2485-44A>G
ENST00000344327.7:c.2485-44A>G	ENSP00000340913.3:n.2485-44A>G
ENST00000348423.8:c.2137-44A>G	ENSP00000343672.4:n.2137-44A>G
ENST00000360497.4:c.2320-44A>G	ENSP00000353687.4:n.2320-44A>G
ENST00000532133.5:c.2251-44A>G	ENSP00000435574.1:n.2251-44A>G
ENST00000532184.1:n.433A>G
NM_004621.5:c.2485-44A>G	NP_004612.2:n.2485-44A>G
XM_006718898.2:c.2410-44A>G	XP_006718961.1:n.2410-44A>G
XM_011542968.1:c.2320-44A>G	XP_011541270.1:n.2320-44A>G
XM_011542969.1:c.2482-40A>G	XP_011541271.1:n.2482-40A>G
XM_011542968.3:c.2320-44A>G	XP_011541270.1:n.2320-44A>G
XM_017018221.2:c.2137-44A>G	XP_016873710.1:n.2137-44A>G
XR_001747948.2:n.2838-40A>G
NM_004621.6:c.2485-44A>G MANE Select	NP_004612.2:n.2485-44A>G