Canonical Allele Identifier: CA227523290

Gene: TRPC6

Linked Data

• dbSNP Id: rs961856281
• gnomAD v4: 11-101488869-G-A
• MyVariant Identifiers: chr11:g.101359600G>A (hg19) ; chr11:g.101488869G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101488869G>A , CM000673.2:g.101488869G>A	GRCh38
NC_000011.9:g.101359600G>A , CM000673.1:g.101359600G>A	GRCh37
NC_000011.8:g.100864810G>A	NCBI36
NG_011476.1:g.100060C>T
NG_011476.2:g.100060C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344327.8:c.1293+68C>T MANE Select	ENSP00000340913.3:n.1293+68C>T
ENST00000344327.7:c.1293+68C>T	ENSP00000340913.3:n.1293+68C>T
ENST00000348423.8:c.946-5704C>T	ENSP00000343672.4:n.946-5704C>T
ENST00000360497.4:c.1128+2687C>T	ENSP00000353687.4:n.1128+2687C>T
ENST00000532133.5:c.1293+68C>T	ENSP00000435574.1:n.1293+68C>T
NM_004621.5:c.1293+68C>T	NP_004612.2:n.1293+68C>T
XM_006718898.2:c.1293+68C>T	XP_006718961.1:n.1293+68C>T
XM_011542968.1:c.1128+68C>T	XP_011541270.1:n.1128+68C>T
XM_011542969.1:c.1293+68C>T	XP_011541271.1:n.1293+68C>T
XM_011542968.3:c.1128+68C>T	XP_011541270.1:n.1128+68C>T
XM_017018221.2:c.946-5704C>T	XP_016873710.1:n.946-5704C>T
XR_001747948.2:n.1649+68C>T
NM_004621.6:c.1293+68C>T MANE Select	NP_004612.2:n.1293+68C>T