Canonical Allele Identifier: CA1995884740
Gene: TRPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101452787T= , CM000673.2:g.101452787T= GRCh38
NC_000011.9:g.101323518T= , CM000673.1:g.101323518T= GRCh37
NC_000011.8:g.100828728T= NCBI36
NG_011476.1:g.136142A=
NG_011476.2:g.136142A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344327.8:c.*168A= MANE Select ENSP00000340913.3:n.*168A=
ENST00000344327.7:c.*168A= ENSP00000340913.3:n.*168A=
NM_004621.5:c.*168A= NP_004612.2:n.*168A=
XM_006718898.2:c.*168A= XP_006718961.1:n.*168A=
XM_011542968.1:c.*168A= XP_011541270.1:n.*168A=
XM_011542968.3:c.*168A= XP_011541270.1:n.*168A=
XM_017018221.2:c.*168A= XP_016873710.1:n.*168A=
XR_001747948.2:n.3321A=
NM_004621.6:c.*168A= MANE Select NP_004612.2:n.*168A=