Canonical Allele Identifier: CA1995831482
Gene: TRPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101473691C= , CM000673.2:g.101473691C= GRCh38
NC_000011.9:g.101344422C= , CM000673.1:g.101344422C= GRCh37
NC_000011.8:g.100849632C= NCBI36
NG_011476.1:g.115238G=
NG_011476.2:g.115238G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344327.8:c.1827G= MANE Select ENSP00000340913.3:p.Arg609=
ENST00000344327.7:c.1827G= ENSP00000340913.3:p.Arg609=
ENST00000348423.8:c.1479G= ENSP00000343672.4:p.Arg493=
ENST00000360497.4:c.1662G= ENSP00000353687.4:p.Arg554=
ENST00000532133.5:c.1593G= ENSP00000435574.1:p.Arg531=
NM_004621.5:c.1827G= NP_004612.2:p.Arg609=
XM_006718898.2:c.1827G= XP_006718961.1:p.Arg609=
XM_011542968.1:c.1662G= XP_011541270.1:p.Arg554=
XM_011542969.1:c.1827G= XP_011541271.1:p.Arg609=
XM_011542968.3:c.1662G= XP_011541270.1:p.Arg554=
XM_017018221.2:c.1479G= XP_016873710.1:p.Arg493=
XR_001747948.2:n.2183G=
NM_004621.6:c.1827G= MANE Select NP_004612.2:p.Arg609=