Canonical Allele Identifier: CA1995875021
Gene: TRPC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101504550G= , CM000673.2:g.101504550G= GRCh38
NC_000011.9:g.101375281G= , CM000673.1:g.101375281G= GRCh37
NC_000011.8:g.100880491G= NCBI36
NG_011476.1:g.84379C=
NG_011476.2:g.84379C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344327.8:c.419C= MANE Select ENSP00000340913.3:p.Ala140=
ENST00000344327.7:c.419C= ENSP00000340913.3:p.Ala140=
ENST00000348423.8:c.419C= ENSP00000343672.4:p.Ala140=
ENST00000360497.4:c.419C= ENSP00000353687.4:p.Ala140=
ENST00000532133.5:c.419C= ENSP00000435574.1:p.Ala140=
NM_004621.5:c.419C= NP_004612.2:p.Ala140=
XM_006718898.2:c.419C= XP_006718961.1:p.Ala140=
XM_011542968.1:c.254C= XP_011541270.1:p.Ala85=
XM_011542969.1:c.419C= XP_011541271.1:p.Ala140=
XM_011542968.3:c.254C= XP_011541270.1:p.Ala85=
XM_017018221.2:c.419C= XP_016873710.1:p.Ala140=
XR_001747948.2:n.775C=
NM_004621.6:c.419C= MANE Select NP_004612.2:p.Ala140=