Canonical Allele Identifier: CA10637222
Gene: TRPC6 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101452287C>T , CM000673.2:g.101452287C>T GRCh38
NC_000011.9:g.101323018C>T , CM000673.1:g.101323018C>T GRCh37
NC_000011.8:g.100828228C>T NCBI36
NG_011476.1:g.136642G>A
NG_011476.2:g.136642G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344327.8:c.*668G>A MANE Select ENSP00000340913.3:n.*668G>A
ENST00000344327.7:c.*668G>A ENSP00000340913.3:n.*668G>A
NM_004621.5:c.*668G>A NP_004612.2:n.*668G>A
XM_006718898.2:c.*668G>A XP_006718961.1:n.*668G>A
XM_011542968.1:c.*668G>A XP_011541270.1:n.*668G>A
XR_947953.1:n.3179C>T
XM_011542968.3:c.*668G>A XP_011541270.1:n.*668G>A
XM_017018221.2:c.*668G>A XP_016873710.1:n.*668G>A
XR_001747948.2:n.3821G>A
NM_004621.6:c.*668G>A MANE Select NP_004612.2:n.*668G>A