Canonical Allele Identifier: CA941545206

Gene: TRPC6

Linked Data

• dbSNP Id: rs1858812509
• gnomAD v3: 11-101453541-T-C
• gnomAD v4: 11-101453541-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101453541T>C , CM000673.2:g.101453541T>C	GRCh38
NC_000011.9:g.101324272T>C , CM000673.1:g.101324272T>C	GRCh37
NC_000011.8:g.100829482T>C	NCBI36
NG_011476.1:g.135388A>G
NG_011476.2:g.135388A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344327.8:c.2644+109A>G MANE Select	ENSP00000340913.3:n.2644+109A>G
ENST00000344327.7:c.2644+109A>G	ENSP00000340913.3:n.2644+109A>G
ENST00000348423.8:c.2296+109A>G	ENSP00000343672.4:n.2296+109A>G
ENST00000360497.4:c.2479+109A>G	ENSP00000353687.4:n.2479+109A>G
ENST00000532133.5:c.2410+109A>G	ENSP00000435574.1:n.2410+109A>G
NM_004621.5:c.2644+109A>G	NP_004612.2:n.2644+109A>G
XM_006718898.2:c.2569+109A>G	XP_006718961.1:n.2569+109A>G
XM_011542968.1:c.2479+109A>G	XP_011541270.1:n.2479+109A>G
XM_011542968.3:c.2479+109A>G	XP_011541270.1:n.2479+109A>G
XM_017018221.2:c.2296+109A>G	XP_016873710.1:n.2296+109A>G
XR_001747948.2:n.3001+109A>G
NM_004621.6:c.2644+109A>G MANE Select	NP_004612.2:n.2644+109A>G