Canonical Allele Identifier: CA1995831517
Community Standard Title: NM_004621.6(TRPC6):c.1766C= (p.Ser589=)
Gene: TRPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101473752G= , CM000673.2:g.101473752G= GRCh38
NC_000011.9:g.101344483G= , CM000673.1:g.101344483G= GRCh37
NC_000011.8:g.100849693G= NCBI36
NG_011476.1:g.115177C=
NG_011476.2:g.115177C=

Transcript Alleles

HGVS Amino-acid Change
NM_004621.6:c.1766C= MANE Select NP_004612.2:p.Ser589=
ENST00000344327.8:c.1766C= MANE Select ENSP00000340913.3:p.Ser589=
NM_004621.5:c.1766C= NP_004612.2:p.Ser589=
ENST00000344327.7:c.1766C= ENSP00000340913.3:p.Ser589=
ENST00000348423.8:c.1418C= ENSP00000343672.4:p.Ser473=
ENST00000360497.4:c.1601C= ENSP00000353687.4:p.Ser534=
ENST00000532133.5:c.1532C= ENSP00000435574.1:p.Ser511=
XM_006718898.2:c.1766C= XP_006718961.1:p.Ser589=
XM_011542968.1:c.1601C= XP_011541270.1:p.Ser534=
XM_011542968.3:c.1601C= XP_011541270.1:p.Ser534=
XM_011542969.1:c.1766C= XP_011541271.1:p.Ser589=
XM_017018221.2:c.1418C= XP_016873710.1:p.Ser473=
XR_001747948.2:n.2122C=