Canonical Allele Identifier: CA1995897707
Gene: TRPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101469451T= , CM000673.2:g.101469451T= GRCh38
NC_000011.9:g.101340182T= , CM000673.1:g.101340182T= GRCh37
NC_000011.8:g.100845392T= NCBI36
NG_011476.1:g.119478A=
NG_011476.2:g.119478A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344327.8:c.2460A= MANE Select ENSP00000340913.3:p.Ser820=
ENST00000344327.7:c.2460A= ENSP00000340913.3:p.Ser820=
ENST00000348423.8:c.2112A= ENSP00000343672.4:p.Ser704=
ENST00000360497.4:c.2295A= ENSP00000353687.4:p.Ser765=
ENST00000532133.5:c.2226A= ENSP00000435574.1:p.Ser742=
NM_004621.5:c.2460A= NP_004612.2:p.Ser820=
XM_006718898.2:c.2409+1732A= XP_006718961.1:n.2409+1732A=
XM_011542968.1:c.2295A= XP_011541270.1:p.Ser765=
XM_011542969.1:c.2460A= XP_011541271.1:p.Ser820=
XM_011542968.3:c.2295A= XP_011541270.1:p.Ser765=
XM_017018221.2:c.2112A= XP_016873710.1:p.Ser704=
XR_001747948.2:n.2816A=
NM_004621.6:c.2460A= MANE Select NP_004612.2:p.Ser820=